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CN114376772A - Interbody fusion cage and method of use - Google Patents

Interbody fusion cage and method of use Download PDF

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Publication number
CN114376772A
CN114376772A CN202011139958.0A CN202011139958A CN114376772A CN 114376772 A CN114376772 A CN 114376772A CN 202011139958 A CN202011139958 A CN 202011139958A CN 114376772 A CN114376772 A CN 114376772A
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auxiliary groove
accommodating part
hole
adsorption layer
bracket
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Inventor
张超
李长青
周跃
郑文杰
黄博
刘明岩
郑卜纵
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Shanghai Sanyou Medical Co ltd
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Shanghai Sanyou Medical Co ltd
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Priority to CN202011139958.0A priority Critical patent/CN114376772A/en
Priority to CN202211329184.7A priority patent/CN115531055A/en
Publication of CN114376772A publication Critical patent/CN114376772A/en
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/44Joints for the spine, e.g. vertebrae, spinal discs
    • A61F2/4455Joints for the spine, e.g. vertebrae, spinal discs for the fusion of spinal bodies, e.g. intervertebral fusion of adjacent spinal bodies, e.g. fusion cages
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L27/00Materials for grafts or prostheses or for coating grafts or prostheses
    • A61L27/28Materials for coating prostheses
    • A61L27/34Macromolecular materials
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L27/00Materials for grafts or prostheses or for coating grafts or prostheses
    • A61L27/50Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
    • A61L27/52Hydrogels or hydrocolloids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L27/00Materials for grafts or prostheses or for coating grafts or prostheses
    • A61L27/50Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
    • A61L27/54Biologically active materials, e.g. therapeutic substances
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30003Material related properties of the prosthesis or of a coating on the prosthesis
    • A61F2002/3006Properties of materials and coating materials
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30621Features concerning the anatomical functioning or articulation of the prosthetic joint
    • A61F2002/30622Implant for fusing a joint or bone material
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30667Features concerning an interaction with the environment or a particular use of the prosthesis
    • A61F2002/30677Means for introducing or releasing pharmaceutical products, e.g. antibiotics, into the body
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/30721Accessories
    • A61F2002/30733Inserts placed into an endoprosthetic cavity, e.g. for modifying a material property
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2300/00Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
    • A61L2300/20Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices containing or releasing organic materials
    • A61L2300/252Polypeptides, proteins, e.g. glycoproteins, lipoproteins, cytokines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2300/00Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
    • A61L2300/20Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices containing or releasing organic materials
    • A61L2300/30Compounds of undetermined constitution extracted from natural sources, e.g. Aloe Vera
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2300/00Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
    • A61L2300/40Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices characterised by a specific therapeutic activity or mode of action
    • A61L2300/412Tissue-regenerating or healing or proliferative agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2300/00Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
    • A61L2300/60Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices characterised by a special physical form
    • A61L2300/606Coatings

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  • Health & Medical Sciences (AREA)
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  • Chemical & Material Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
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  • Transplantation (AREA)
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  • Neurology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Molecular Biology (AREA)
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  • Heart & Thoracic Surgery (AREA)
  • Vascular Medicine (AREA)
  • Prostheses (AREA)

Abstract

本发明提供一种椎间融合器及其使用方法,包括:容纳部,所述容纳部可撑开,所述容纳部上设有开口,所述容纳部的外侧面上包覆有药物吸附层,所述药物吸附层的材料为医用凝胶;所述药物吸附层所吸附的药物为能够吸附促进骨生长的物质。本发明的椎间融合器具有可以微创植入,骨结合能力好,融合更彻底,术后即时稳定性好,创伤小、出血少、术后恢复快等优点。

Figure 202011139958

The present invention provides an intervertebral fusion cage and a method of using the same, comprising: a accommodating part, the accommodating part can be stretched, the accommodating part is provided with an opening, and the outer surface of the accommodating part is covered with a drug adsorption layer , the material of the drug adsorption layer is medical gel; the drug adsorbed by the drug adsorption layer is a substance that can adsorb and promote bone growth. The intervertebral fusion device of the invention has the advantages of minimally invasive implantation, good osseointegration ability, more complete fusion, good immediate postoperative stability, less trauma, less bleeding, and quick postoperative recovery.

Figure 202011139958

Description

椎间融合器及其使用方法Interbody cage and method of use

技术领域technical field

本发明涉及植入器械技术领域,特别是涉及一种椎间融合器及其使用方法。The present invention relates to the technical field of implanted instruments, in particular to an intervertebral cage and a method of using the same.

背景技术Background technique

在常见的椎间融合手术中,椎间融合器是当前椎间融合手术最常用的装置。根据其手术入路不同,后方入路常用子弹头型融合器;侧后方入路常用肾型融合器;前方入路和侧前方入路用楔形融合器。当前的融合器材料为聚醚醚酮,它的骨结合能力差,植入体内之后,聚醚醚酮本身不会有骨长入,所以后期的融合主要靠植骨。另外,由于微创手术具有切口小、软组织损伤小、出血少、术后康复快等优点成为当前脊柱外科手术的热门发展方向。如何涉及一种骨结合能力好,可以微创植入的椎间融合器是本领域技术人员需要解决的问题。In the common interbody fusion surgery, the interbody cage is the most commonly used device in the current interbody fusion surgery. According to the different surgical approaches, bullet-shaped cages are commonly used for the posterior approach; renal-type cages are commonly used for the lateral-posterior approach; and wedge-shaped cages are used for the anterior approach and the lateral-anterior approach. The current cage material is polyetheretherketone, which has poor osseointegration ability. After implantation, polyetheretherketone itself will not have bone ingrowth, so the later fusion mainly relies on bone grafting. In addition, minimally invasive surgery has the advantages of small incision, small soft tissue damage, less bleeding, and quick postoperative recovery, which has become a popular development direction of current spine surgery. How to relate to an intervertebral cage with good osseointegration ability and minimally invasive implantation is a problem to be solved by those skilled in the art.

发明内容SUMMARY OF THE INVENTION

鉴于以上所述现有技术的缺点,本发明解决的技术问题在于提供一种的椎间融合器。In view of the above-mentioned shortcomings of the prior art, the technical problem solved by the present invention is to provide an intervertebral cage.

为实现上述目的及其他相关目的,本发明提供一种椎间融合器,包括:容纳部,所述容纳部可撑开,所述容纳部上设有开口,所述容纳部的外侧面上包覆有药物吸附层。In order to achieve the above object and other related objects, the present invention provides an intervertebral cage, comprising: a accommodating part, the accommodating part can be stretched, the accommodating part is provided with an opening, and the outer side of the accommodating part is covered with Covered with a drug adsorption layer.

优选地,所述药物吸附层的材料为医用凝胶。Preferably, the material of the drug adsorption layer is medical gel.

进一步地,所述药物吸附层所吸附的药物为能够吸附促进骨生长的药物。Further, the drug adsorbed by the drug adsorption layer is a drug capable of adsorbing and promoting bone growth.

本发明还涉及一种椎间融合器,包括:容纳部,所述容纳部可撑开,所述容纳部上设有开口,所述容纳部的外侧面上包覆有药物吸附层,所述药物吸附层的材料为医用凝胶;所述药物吸附层所吸附的药物为能够吸附促进骨生长的药物。The present invention also relates to an intervertebral cage, comprising: an accommodating part, the accommodating part can be stretched, an opening is provided on the accommodating part, the outer surface of the accommodating part is covered with a drug adsorption layer, and the The material of the drug adsorption layer is medical gel; the drug adsorbed by the drug adsorption layer is a drug capable of adsorbing and promoting bone growth.

优选地,所述药物吸附层所吸附的药物为骨形态发生蛋白或者干细胞。Preferably, the drug adsorbed by the drug adsorption layer is bone morphogenetic protein or stem cells.

优选地,所述容纳部为囊袋。Preferably, the accommodating portion is a pouch.

优选地,所述的椎间融合器,还包括连接杆,所述连接杆的一端与所述开口连接,沿着所述连接杆的轴向设有中间通孔,所述中间通孔与所述开口连通。Preferably, the intervertebral cage further includes a connecting rod, one end of the connecting rod is connected to the opening, and a middle through hole is provided along the axial direction of the connecting rod, and the middle through hole is connected to the opening. The opening is connected.

优选地,所述的椎间融合器,还包括撑开支架,所述撑开支架可插入于所述容纳部中;所述撑开支架包括:支架主体和支撑杆;Preferably, the intervertebral cage further includes a spreader bracket, which can be inserted into the accommodating portion; the spreader bracket includes: a bracket main body and a support rod;

所述支架主体为长条状结构,所述支架主体的外周侧面包括依次连接的第一开槽面、第一支撑面、第二开槽面和第二支撑面;所述第一开槽面与所述第二开槽面相对设置;所述第一支撑面与所述第二支撑面相对设置;The bracket body is a long strip structure, and the outer peripheral side surface of the bracket body includes a first slotted surface, a first support surface, a second slotted surface and a second support surface connected in sequence; the first slotted surface opposite to the second slotted surface; the first support surface and the second support surface are arranged opposite;

所述支架主体在长度方向上的前端上设有安装部,所述支架主体在长度方向上的后端上设有驱动部;The front end of the bracket body in the longitudinal direction is provided with a mounting portion, and the rear end of the bracket body in the longitudinal direction is provided with a driving portion;

所述支架主体上设有贯通孔,所述贯通孔的两端分别贯通至所述安装部的前端和所述驱动部的后端,所述贯通孔的轴向与所述支架主体的长度方向同向;The bracket body is provided with a through hole, two ends of the through hole respectively penetrate to the front end of the mounting part and the rear end of the driving part, and the axial direction of the through hole is the same as the length direction of the bracket body. In the same direction;

所述支撑杆依次穿过所述安装部、所述支架主体和所述驱动部,所述支撑杆与所述贯通孔为间隙配合,所述支撑杆与所述安装部固定连接;所述支撑杆具有中空通道,所述中空通道贯通至所述支撑杆的后端;The support rod passes through the installation part, the bracket main body and the driving part in sequence, the support rod and the through hole are in clearance fit, and the support rod is fixedly connected with the installation part; the support rod The rod has a hollow channel, and the hollow channel penetrates to the rear end of the support rod;

在所述第一开槽面上的宽度方向上的中部具有中间长条槽,所述中间长条槽贯通至所述第二开槽面,所述中间长条槽的长度方向与所述第一开槽面的长度方向同向;The middle part of the first grooved surface in the width direction has a middle long groove, the middle long groove penetrates to the second grooved surface, and the length direction of the middle long groove is the same as that of the first grooved surface. The length direction of a slotted surface is in the same direction;

沿着所述第一开槽面上的宽度方向,在所述中间长条槽的两侧分别设有第一辅助槽组和第二辅助槽组;所述第一辅助槽组和所述第二辅助槽组的结构相同,所述第一辅助槽组包括沿着所述第一开槽面上的长度方向依次设置的前端辅助槽和后端辅助槽,所述前端辅助槽和所述后端辅助槽之间具有间隔,所述前端辅助槽的后端与所述后端辅助槽的前端之间的连线的中点连接所述中间长条槽的长度的中点的连线与所述支架主体的宽度方向同向;Along the width direction of the first slotted surface, a first auxiliary slot group and a second auxiliary slot group are respectively provided on both sides of the middle elongated slot; the first auxiliary slot group and the first auxiliary slot group are respectively provided. The structures of the two auxiliary groove groups are the same. The first auxiliary groove group includes a front-end auxiliary groove and a rear-end auxiliary groove arranged in sequence along the length direction of the first slotted surface. There is a space between the end auxiliary grooves, and the midpoint of the connection line between the rear end of the front end auxiliary groove and the front end of the rear end auxiliary groove connects the connection line of the midpoint of the length of the middle elongated groove and the end point. The width directions of the main body of the bracket are in the same direction;

所述第一支撑面通过第一连接块与第一支撑板连接;所述第二支撑面通过第二连接块与第二支撑板连接;The first support surface is connected with the first support plate through a first connection block; the second support surface is connected with the second support plate through a second connection block;

所述支撑杆的外侧壁上具有侧壁通孔,所述侧壁通孔与所述中空通道连通,所述侧壁通孔处于所述贯通孔与所述中间长条槽连通所构成的主腔室中,且将所述支架主体的前端和后端相比较,所述侧壁通孔较靠近所述支架主体的前端;The outer side wall of the support rod is provided with a side wall through hole, the side wall through hole communicates with the hollow channel, and the side wall through hole is in the main part formed by the communication between the through hole and the middle elongated slot. in the chamber, and comparing the front end and the rear end of the bracket body, the side wall through hole is closer to the front end of the bracket body;

顶住所述支撑杆的前端,推动所述驱动部向着靠近所述安装部的方向移动,所述支架主体伸展为六边形结构。The front end of the support rod is pressed to push the driving part to move toward the direction close to the installation part, and the bracket body extends into a hexagonal structure.

优选地,所述的椎间融合器,还包括撑开部件,所述撑开部件为弹性板件,所述弹性板件卷曲回转形成由内至外依次环绕的多个圈层结构,所有圈层结构的中轴线共线。Preferably, the intervertebral cage further includes a spreading member, the spreading member is an elastic plate member, and the elastic plate member is curled and turned to form a plurality of ring-layer structures that are sequentially surrounded from the inside to the outside. The central axis of the layer structure is collinear.

本发明还涉及一种椎间融合器的使用方法,将权利要求中所述的椎间融合器的药物吸附层浸泡在骨形态发生蛋白或者干细胞中,使得所述药物吸附层吸附骨形态发生蛋白或者干细胞。The present invention also relates to a method for using an intervertebral cage. The drug adsorption layer of the intervertebral cage described in the claims is soaked in bone morphogenetic protein or stem cells, so that the drug adsorption layer adsorbs the bone morphogenetic protein. or stem cells.

如上所述,本发明的椎间融合器及其使用方法,具有以下有益效果:As mentioned above, the intervertebral cage of the present invention and its using method have the following beneficial effects:

本发明的椎间融合器中,容纳部在未撑开时进入人体,当容纳部达到椎体之间后,容纳部再撑开;则该椎间融合器可以微创手术的方式经小通道植入中;容纳部的外侧面上包覆有药物吸附层,药物吸附层在术前浸入促进骨生长的物质中,则药物吸附层能够吸附促进骨生长的物质;待容纳部在椎体之间撑开后,药物吸附层能够附着在椎体之间,药物吸附层上的促进骨生长的物质能够提高骨的结合能力;本发明为一种带涂层的椎间融合装置,本发明的椎间融合器具有可以微创植入,骨结合能力好,融合更彻底,术后即时稳定性好,创伤小、出血少、术后恢复快等优点。In the intervertebral cage of the present invention, the accommodating part enters the human body when it is not stretched, and when the accommodating part reaches between the vertebral bodies, the accommodating part is stretched again; then the intervertebral cage can be operated through a small channel in a minimally invasive manner During implantation; the outer surface of the accommodating part is covered with a drug adsorption layer, and the drug adsorption layer is immersed in the substance that promotes bone growth before operation, and the drug adsorption layer can absorb the substance that promotes bone growth; After the intervertebral space is opened, the drug adsorption layer can be attached between the vertebral bodies, and the bone growth-promoting substance on the drug adsorption layer can improve the binding ability of the bone; the present invention is a coated intervertebral fusion device, and the The intervertebral cage has the advantages of minimally invasive implantation, good osseointegration, more complete fusion, good immediate stability after surgery, less trauma, less bleeding, and faster postoperative recovery.

附图说明Description of drawings

图1显示为实施例1的椎间融合器插入椎体之间的结构示意图。Fig. 1 is a schematic diagram showing the structure of the intervertebral cage inserted between the vertebral bodies of Example 1.

图2显示为实施例1的椎间融合器的立体结构示意图。FIG. 2 is a schematic diagram of the three-dimensional structure of the interbody cage of Example 1. FIG.

图3显示为实施例1的椎间融合器的内部结构示意图。FIG. 3 is a schematic diagram showing the internal structure of the interbody cage of Example 1. FIG.

图4显示为实施例2的椎间融合器的容纳部的内部插入撑开支架时的结构示意图。FIG. 4 is a schematic diagram showing the structure of the accommodating part of the intervertebral cage of Example 2 when a distraction bracket is inserted.

图5显示为实施例2的椎间融合器的撑开支架处于初始状态的侧面立体结构示意图。FIG. 5 is a schematic side view of the three-dimensional structure of the distraction bracket of the intervertebral cage of Example 2 in an initial state.

图6显示为实施例2的椎间融合器的撑开支架处于初始状态的前侧立体结构示意图。FIG. 6 is a schematic diagram showing the front side three-dimensional structure of the distraction bracket of the intervertebral cage of Example 2 in an initial state.

图7显示为实施例2的椎间融合器的撑开支架处于初始状态的后侧立体结构示意图。FIG. 7 is a schematic diagram showing the rear side three-dimensional structure of the distraction bracket of the intervertebral cage of Example 2 in an initial state.

图8显示为实施例2的椎间融合器的撑开支架处于初始状态的侧面结构示意图。FIG. 8 is a schematic side view of the structure of the distraction bracket of the intervertebral cage of Example 2 in an initial state.

图9显示为图8的A-A剖面结构示意图。FIG. 9 is a schematic diagram showing the cross-sectional structure of A-A of FIG. 8 .

图10显示为实施例2的椎间融合器的撑开支架的支架主体处于初始状态的侧面结构示意图。FIG. 10 is a schematic side view of the structure of the stent body of the distracting stent of the intervertebral cage of Example 2 in an initial state.

图11显示为图10的B-B剖面结构示意图。FIG. 11 is a schematic diagram of the cross-sectional structure taken along the line B-B of FIG. 10 .

图12显示为实施例2的椎间融合器的撑开支架的支撑杆的立体结构示意图。FIG. 12 is a schematic three-dimensional structural diagram of the support rod of the distraction bracket of the intervertebral cage of Example 2. FIG.

图13显示为实施例2的椎间融合器的撑开支架的处于展开状态的立体侧面结构示意图。FIG. 13 is a schematic three-dimensional side structure view of the distraction bracket of the intervertebral cage of Example 2 in a deployed state.

图14显示为实施例3的椎间融合器的撑开部件的处于收紧状态的立体结构示意图。FIG. 14 is a schematic three-dimensional structural diagram of the distraction component of the intervertebral cage of Example 3 in a tightened state.

图15显示为实施例3的椎间融合器的撑开部件的处于舒展状态的立体结构示意图。FIG. 15 is a schematic three-dimensional structural diagram of the distraction component of the interbody cage of Example 3 in a stretched state.

附图标号说明Explanation of reference numerals

10 容纳部10 Housing

11 开口11 opening

20 药物吸附层20 Drug adsorption layer

30 连接杆30 connecting rod

31 中间通孔31 Middle through hole

100 支架主体100 Bracket body

101 第一开槽面101 First grooved surface

102 第一支撑面102 First support surface

103 第二开槽面103 Second grooved surface

104 第二支撑面104 Second support surface

110 安装部110 Installation part

111 前缩结构111 Front indentation structure

120 驱动部120 Drive

121 卡槽121 card slot

130 贯通孔130 Through hole

140 中间长条槽140 Middle slot

150 第一辅助槽组150 First Auxiliary Slot Group

151 前端辅助槽151 Front Auxiliary Slot

152 后端辅助槽152 Rear auxiliary slot

153 前槽部前凹陷结构153 Front recessed structure of front groove

154 前槽部后凹陷结构154 Front groove rear recessed structure

155 后槽部前凹陷结构155 Front recessed structure of rear groove

156 后槽部后凹陷结构156 Rear recessed structure of the rear groove

160 第二辅助槽组160 Second auxiliary slot group

171 第一连接块171 First connection block

172 第二连接块172 Second connection block

181 第一支撑板181 First support plate

182 第二支撑板182 Second support plate

183 第一斜面183 First Bevel

184 第二斜面184 Second slope

200 支撑杆200 support rod

210 中空通道210 Hollow channel

220 侧壁通孔220 Sidewall Through Holes

230 内连接部230 inner connector

240 外连接部240 Outer connector

300 撑开部件300 spread parts

310 圈层结构310 Circle Structure

具体实施方式Detailed ways

以下由特定的具体实施例说明本发明的实施方式,熟悉此技术的人士可由本说明书所揭露的内容轻易地了解本发明的其他优点及功效。The embodiments of the present invention are described below by specific embodiments, and those skilled in the art can easily understand other advantages and effects of the present invention from the contents disclosed in this specification.

请参阅附图。须知,本说明书所附图式所绘示的结构、比例、大小等,均仅用以配合说明书所揭示的内容,以供熟悉此技术的人士了解与阅读,并非用以限定本发明可实施的限定条件,故不具技术上的实质意义,任何结构的修饰、比例关系的改变或大小的调整,在不影响本发明所能产生的功效及所能达成的目的下,均应仍落在本发明所揭示的技术内容得能涵盖的范围内。同时,本说明书中所引用的如“上”、“下”、“左”、“右”、“中间”及“一”等的用语,亦仅为便于叙述的明了,而非用以限定本发明可实施的范围,其相对关系的改变或调整,在无实质变更技术内容下,当亦视为本发明可实施的范畴。Please see attached image. It should be noted that the structures, proportions, sizes, etc. shown in the drawings in this specification are only used to cooperate with the contents disclosed in the specification, so as to be understood and read by those who are familiar with the technology, and are not used to limit the implementation of the present invention. Restricted conditions, it does not have technical substantive significance, any structural modification, proportional relationship change or size adjustment, without affecting the effect that the present invention can produce and the purpose that can be achieved, should still fall within the present invention. The disclosed technical content must be within the scope of coverage. At the same time, the terms such as "up", "down", "left", "right", "middle" and "one" quoted in this specification are only for the convenience of description and clarity, and are not used to limit this specification. The implementable scope of the invention, and the change or adjustment of the relative relationship thereof, shall also be regarded as the implementable scope of the present invention without substantially changing the technical content.

实施例1Example 1

如图1至图3所示,本实施例的椎间融合器,包括:容纳部10,容纳部10可撑开,容纳部10上设有开口11,容纳部10的外侧面上包覆有药物吸附层20,药物吸附层20的材料为医用凝胶。As shown in FIG. 1 to FIG. 3 , the intervertebral cage of this embodiment includes: an accommodating part 10 , the accommodating part 10 can be stretched, an opening 11 is provided on the accommodating part 10 , and the outer surface of the accommodating part 10 is covered with The drug adsorption layer 20 is made of medical gel.

本发明的椎间融合器中,容纳部10在未撑开时进入人体,当容纳部10达到椎体之间后,容纳部10再撑开;则该椎间融合器可以微创手术的方式经小通道植入中;容纳部10的外侧面上包覆有药物吸附层20,药物吸附层20的材料为医用凝胶,药物吸附层20在术前浸入促进骨生长的物质中,则药物吸附层20能够吸附促进骨生长的物质;待容纳部10在椎体之间撑开后,药物吸附层20能够附着在椎体之间,药物吸附层20上的促进骨生长的物质能够提高骨的结合能力;本发明为一种带涂层的椎间融合装置,本发明的椎间融合器具有可以微创植入,骨结合能力好,融合更彻底,术后即时稳定性好,创伤小、出血少、术后恢复快等优点。本发明的椎间融合器可应用于椎间盘镜手术中。本实施例中的医用凝胶的材料为透明质酸钠。药物吸附层20所吸附的药物为能够吸附促进骨生长的物质。本实施例中,药物吸附层20所的能够吸附促进骨生长的物质为骨形态发生蛋白或者干细胞。In the intervertebral cage of the present invention, the accommodating portion 10 enters the human body when it is not stretched, and when the accommodating portion 10 reaches between the vertebral bodies, the accommodating portion 10 is stretched again; the intervertebral cage can be operated in a minimally invasive manner It is implanted through a small channel; the outer surface of the accommodating part 10 is covered with a drug adsorption layer 20, and the material of the drug adsorption layer 20 is medical gel. The adsorption layer 20 can adsorb substances that promote bone growth; after the accommodating portion 10 is stretched between the vertebral bodies, the drug adsorption layer 20 can be attached between the vertebral bodies, and the substance that promotes bone growth on the drug adsorption layer 20 can improve bone growth. The present invention is a coated intervertebral fusion device, the intervertebral fusion device of the present invention has the advantages of minimally invasive implantation, good osseointegration ability, more thorough fusion, good immediate stability after operation, and less trauma. , less bleeding, faster postoperative recovery and so on. The intervertebral cage of the present invention can be applied to the endoscopic surgery of the intervertebral disc. The material of the medical gel in this embodiment is sodium hyaluronate. The drug adsorbed by the drug adsorption layer 20 is a substance capable of adsorbing and promoting bone growth. In this embodiment, the substance capable of adsorbing and promoting bone growth on the drug adsorption layer 20 is bone morphogenetic protein or stem cells.

容纳部10为囊袋。通过囊袋的开口11,对囊袋中通入生理盐水或者充入气体即可使囊袋撑开。The accommodating portion 10 is a pouch. Through the opening 11 of the capsular bag, the capsular bag can be opened by passing physiological saline or inflating gas into the capsular bag.

本实施例的椎间融合器的使用方法,包括以下步骤:The method of using the intervertebral cage of the present embodiment includes the following steps:

1)将椎间融合器的药物吸附层20浸泡在骨形态发生蛋白或者干细胞中,使得所述药物吸附层20吸附骨形态发生蛋白或者干细胞;1) soaking the drug adsorption layer 20 of the interbody cage in bone morphogenetic protein or stem cells, so that the drug adsorption layer 20 adsorbs bone morphogenetic protein or stem cells;

2)当容纳部10达到椎体之间后,对囊袋中通入生理盐水或者充入气体,使囊袋被撑开。2) After the accommodating portion 10 reaches between the vertebral bodies, the pouch is filled with physiological saline or gas to be opened.

实施例2Example 2

如图4至图13所示,本实施例中,椎间融合器,还包括连接杆30,连接杆30的一端与开口11连接,沿着连接杆30的轴向设有中间通孔31,中间通孔31与开口11连通。连接杆30的设置使得椎间融合器的结构更稳定,更易于操作。As shown in FIGS. 4 to 13 , in this embodiment, the intervertebral cage further includes a connecting rod 30 , one end of the connecting rod 30 is connected to the opening 11 , and an intermediate through hole 31 is provided along the axial direction of the connecting rod 30 , The middle through hole 31 communicates with the opening 11 . The arrangement of the connecting rod 30 makes the structure of the intervertebral cage more stable and easier to operate.

椎间融合器,还包括撑开支架,撑开支架可插入于容纳部10中;撑开支架可插入于容纳部10中;撑开支架包括:支架主体100和支撑杆200,支架主体100和支撑杆200均采用钛制成;支架主体100为长条状结构,支架主体100的外周侧面包括依次连接的第一开槽面101、第一支撑面102、第二开槽面103和第二支撑面104;第一开槽面101与第二开槽面103相对设置;第一支撑面102与第二支撑面104相对设置;The intervertebral cage also includes a spreader bracket, which can be inserted into the accommodating part 10; the spreader bracket can be inserted into the accommodating part 10; the spreader bracket includes: a bracket main body 100 and a support rod 200, the bracket main body 100 and The support rods 200 are all made of titanium; the bracket body 100 is a long strip structure, and the outer peripheral side of the bracket body 100 includes a first slotted surface 101 , a first support surface 102 , a second slotted surface 103 and a second slotted surface 101 connected in sequence. The supporting surface 104; the first slotted surface 101 is arranged opposite to the second slotted surface 103; the first supporting surface 102 is arranged opposite to the second supporting surface 104;

支架主体100在长度方向上的前端上设有安装部110,支架主体100在长度方向上的后端上设有驱动部120;A mounting portion 110 is provided on the front end of the bracket body 100 in the longitudinal direction, and a driving portion 120 is provided on the rear end of the bracket body 100 in the longitudinal direction;

支架主体100上设有贯通孔130,贯通孔130的两端分别贯通至安装部110的前端和驱动部120的后端,贯通孔130的轴向与支架主体100的长度方向同向;The bracket main body 100 is provided with a through hole 130, two ends of the through hole 130 respectively penetrate to the front end of the mounting part 110 and the rear end of the driving part 120, and the axial direction of the through hole 130 is the same as the longitudinal direction of the bracket main body 100;

支撑杆200依次穿过安装部110、支架主体100和驱动部120,支撑杆200与贯通孔130为间隙配合,支撑杆200与安装部110固定连接;支撑杆200具有中空通道210,中空通道210贯通至支撑杆200的后端;中空通道210的轴向与支撑杆200的轴向同向;The support rod 200 passes through the mounting part 110 , the bracket main body 100 and the driving part 120 in sequence, the support rod 200 and the through hole 130 are clearance fit, and the support rod 200 is fixedly connected with the mounting part 110 ; the support rod 200 has a hollow channel 210 , and the hollow channel 210 penetrates to the rear end of the support rod 200; the axial direction of the hollow channel 210 is the same as the axial direction of the support rod 200;

在第一开槽面101上的宽度方向上的中部具有中间长条槽140,中间长条槽140贯通至第二开槽面103,中间长条槽140的长度方向与第一开槽面101的长度方向同向;There is a middle elongated groove 140 in the middle in the width direction on the first slotted surface 101 , the middle elongated slot 140 penetrates to the second slotted surface 103 , and the length direction of the middle elongated slot 140 is the same as that of the first slotted surface 101 . The length direction is the same;

沿着第一开槽面101上的宽度方向,在中间长条槽140的两侧分别设有第一辅助槽组150和第二辅助槽组160;第一辅助槽组150和第二辅助槽组160的结构相同,第一辅助槽组150包括沿着第一开槽面101上的长度方向依次设置的前端辅助槽151和后端辅助槽152,前端辅助槽151和后端辅助槽152之间具有间隔,前端辅助槽151的后端与后端辅助槽152的前端之间的连线的中点连接中间长条槽140的长度的中点的连线为中间连线,该中间连线与支架主体100的宽度W2方向同向;Along the width direction of the first slotted surface 101, a first auxiliary slot group 150 and a second auxiliary slot group 160 are respectively provided on both sides of the middle elongated slot 140; the first auxiliary slot group 150 and the second auxiliary slot group The structure of the group 160 is the same. The first auxiliary groove group 150 includes a front auxiliary groove 151 and a rear auxiliary groove 152 arranged in sequence along the length direction of the first slotted surface 101. There is a space between them, and the line connecting the midpoint of the connection line between the rear end of the front end auxiliary groove 151 and the front end of the rear end auxiliary groove 152 and the middle point of the length of the middle elongated groove 140 is the middle connection line, and the middle connection line In the same direction as the width W2 of the bracket body 100;

第一支撑面102通过第一连接块171与第一支撑板181连接;第二支撑面104通过第二连接块172与第二支撑板182连接;The first support surface 102 is connected with the first support plate 181 through the first connection block 171; the second support surface 104 is connected with the second support plate 182 through the second connection block 172;

支撑杆200的外侧壁上具有侧壁通孔220,侧壁通孔220与中空通道210连通,侧壁通孔220处于贯通孔130与中间长条槽140连通所构成的主腔室中,且将支架主体100的前端和后端相比较,侧壁通孔220较靠近支架主体100的前端;The outer side wall of the support rod 200 has a side wall through hole 220, the side wall through hole 220 communicates with the hollow channel 210, the side wall through hole 220 is in the main chamber formed by the communication between the through hole 130 and the middle elongated groove 140, and Comparing the front end and rear end of the bracket body 100, the side wall through hole 220 is closer to the front end of the bracket body 100;

顶住支撑杆200的前端,推动驱动部120向着靠近安装部110的方向移动,支架主体100伸展为六边形结构。The front end of the support rod 200 is pushed against the front end of the support rod 200 to push the driving part 120 to move toward the direction close to the installation part 110 , and the bracket main body 100 extends into a hexagonal structure.

本实施例的撑开支架使用时,未撑开的撑开支架设置于未撑开的容纳部10中,当需要撑开容纳部10时,顶住支撑杆200的前端,推动驱动部120向着靠近安装部110的方向移动,支架主体100伸展为六边形结构。本实施例的撑开支架采用钛材料制成,钛材料的使用能够保证有足够的强度维持椎体正常形态。撑开支架用于撑开容纳部。When the spreader bracket of this embodiment is used, the unstretched spreader bracket is arranged in the unstretched accommodating part 10 , when the accommodating part 10 needs to be opened, the front end of the support rod 200 is pressed against the front end of the support rod 200 to push the driving part 120 toward Moving in a direction close to the mounting portion 110 , the bracket body 100 extends into a hexagonal structure. The expansion bracket of this embodiment is made of titanium material, and the use of titanium material can ensure sufficient strength to maintain the normal shape of the vertebral body. The spreading bracket is used for spreading the receiving portion.

第一开槽面101、第一支撑面102、第二开槽面103和第二支撑面104均为平面;第一开槽面101与第二开槽面103相对且平行设置;第一支撑面102与第二支撑面104相对且平行设置;第一支撑面102与第一支撑板181的外侧面平行,第二支撑面104与第二支撑板182的外侧面平行。The first slotted surface 101, the first support surface 102, the second slotted surface 103 and the second support surface 104 are all planes; the first slotted surface 101 and the second slotted surface 103 are opposite and parallel to each other; the first support The surface 102 is opposite and parallel to the second supporting surface 104 ; the first supporting surface 102 is parallel to the outer surface of the first supporting plate 181 , and the second supporting surface 104 is parallel to the outer surface of the second supporting plate 182 .

由于在中间长条槽140的两侧分别设有第一辅助槽组150和第二辅助槽组160;第一辅助槽组150和第二辅助槽组160的结构相同,第一辅助槽组150包括沿着第一开槽面101上的长度方向依次设置的前端辅助槽151和后端辅助槽152,该结构便于支架主体100伸展开。Because the first auxiliary groove group 150 and the second auxiliary groove group 160 are respectively provided on both sides of the middle elongated groove 140; the first auxiliary groove group 150 and the second auxiliary groove group 160 have the same structure, and the first auxiliary groove group 150 The front end auxiliary groove 151 and the rear end auxiliary groove 152 are provided in sequence along the length direction of the first slotted surface 101 , and the structure is convenient for the stent main body 100 to be extended.

第一支撑面102通过第一连接块171与第一支撑板181连接;第二支撑面104通过第二连接块172与第二支撑板182连接,该结构使得第一支撑面102与第一支撑板181之间不接触,第二支撑面104与第二支撑板182之间不接触,则支架主体100伸展开时,第一支撑板181和第二支撑板182能够实现稳定地支撑力。The first support surface 102 is connected to the first support plate 181 through the first connection block 171 ; the second support surface 104 is connected to the second support plate 182 through the second connection block 172 , and the structure makes the first support surface 102 and the first support plate 182 connected. There is no contact between the plates 181 and no contact between the second support surface 104 and the second support plate 182, so when the bracket body 100 is stretched out, the first support plate 181 and the second support plate 182 can achieve a stable support force.

由于前端辅助槽151和后端辅助槽152之间具有间隔,前端辅助槽151的后端与后端辅助槽152的前端之间的连线的中点连接中间长条槽140的长度的中点的连线与支架主体100的宽度W2方向同向。该结构便于支架主体100伸展开形成六边形结构。Since there is a space between the front end auxiliary groove 151 and the rear end auxiliary groove 152 , the midpoint of the line connecting the rear end of the front end auxiliary groove 151 and the front end of the rear end auxiliary groove 152 is connected to the middle point of the length of the middle elongated groove 140 The connection line is in the same direction as the width W2 of the bracket body 100 . This structure facilitates the expansion of the stent body 100 to form a hexagonal structure.

通过前端辅助槽151的后端与后端辅助槽152的前端之间的连线的中点且垂直于支架主体100的长度方向的平面为支架主体100的竖向中间平面,第一连接块171的在长度方向上的两端与竖向中间平面的距离相等,第二连接块172的在长度方向上的两端与竖向中间平面的距离相等。前端辅助槽151与后端辅助槽152之间的间隔的长度方向上的中部的位置与第一连接块171的长度方向上的中部的位置相应;前端辅助槽151与后端辅助槽152之间的间隔的长度方向上的中部的位置与第二连接块172的长度方向上的中部的位置相应;由于第一连接块171增强了第一辅助槽组150的前端辅助槽151与后端辅助槽152之间的间隔处的强度,则有利于第一辅助槽组150的前端辅助槽151与后端辅助槽152之间的间隔处能够在支架主体100伸展为六边形结构的过程中,作为六边形结构的其中一条边;由于第二连接块172增强了第二辅助槽组160的前端辅助槽151与后端辅助槽152之间的间隔处的强度,则有利于第二辅助槽组160的前端辅助槽151与后端辅助槽152之间的间隔处能够在支架主体100伸展为六边形结构的过程中,作为六边形结构的其中一条边。The plane passing through the midpoint of the line between the rear end of the front end auxiliary groove 151 and the front end of the rear end auxiliary groove 152 and perpendicular to the length direction of the bracket main body 100 is the vertical middle plane of the bracket main body 100 . The first connecting block 171 Both ends of the second connecting block 172 in the length direction are at the same distance from the vertical middle plane, and both ends of the second connecting block 172 in the length direction are the same distance from the vertical middle plane. The position of the middle part in the longitudinal direction of the interval between the front end auxiliary groove 151 and the rear end auxiliary groove 152 corresponds to the position of the middle part in the length direction of the first connecting block 171 ; between the front end auxiliary groove 151 and the rear end auxiliary groove 152 The position of the middle part in the length direction of the interval corresponds to the position of the middle part in the length direction of the second connecting block 172; since the first connecting block 171 strengthens the front auxiliary groove 151 and the rear auxiliary groove of the first auxiliary groove group 150 The strength at the interval between 152 is beneficial for the interval between the front auxiliary groove 151 and the rear auxiliary groove 152 of the first auxiliary groove group 150 to be able to act as a One side of the hexagonal structure; since the second connecting block 172 enhances the strength of the interval between the front auxiliary groove 151 and the rear auxiliary groove 152 of the second auxiliary groove group 160, it is beneficial to the second auxiliary groove group The interval between the front end auxiliary groove 151 and the rear end auxiliary groove 152 of 160 can be used as one side of the hexagonal structure during the process of extending the bracket body 100 into the hexagonal structure.

第一支撑板181的在长度方向上的两端与竖向中间平面的距离相等,第二支撑板182的在长度方向上的两端与竖向中间平面的距离相等。该结构使得第一支撑板181和第二支撑板182受到稳定的支撑力。Both ends of the first support plate 181 in the length direction are the same distance from the vertical middle plane, and both ends of the second support plate 182 in the length direction are the same distance from the vertical middle plane. This structure allows the first support plate 181 and the second support plate 182 to receive a stable support force.

第一支撑板181与第二支撑板182的宽度相等,支架主体100的宽度W2小于等于第一支撑板181的宽度。本实施例中,支架主体100的宽度W2等于第一支撑板181的宽度。该结构使得第一支撑板181与第二支撑板182具有较好的支撑力。The widths of the first support plate 181 and the second support plate 182 are equal, and the width W2 of the bracket body 100 is less than or equal to the width of the first support plate 181 . In this embodiment, the width W2 of the bracket body 100 is equal to the width of the first support plate 181 . This structure enables the first support plate 181 and the second support plate 182 to have better supporting force.

第一支撑板181的外侧面与第二支撑板182的外侧面平行;第一支撑板181的外侧面与第二支撑板182的外侧面之间的距离为图8的H所示。The outer surface of the first support plate 181 is parallel to the outer surface of the second support plate 182 ; the distance between the outer surface of the first support plate 181 and the outer surface of the second support plate 182 is shown in H in FIG. 8 .

安装部110的前部为向前收缩的前缩结构111,前缩结构111的前端的圆弧形端面。该结构使得安装部110的前部形成子弹头的形状,便于插入安装。The front part of the installation part 110 is a forward retraction structure 111 that is retracted forward, and the front end of the front retraction structure 111 is an arc-shaped end surface. This structure makes the front part of the installation part 110 form the shape of a bullet, which is convenient for insertion and installation.

前缩结构111的外侧面上具有两个相对设置的前缩部斜面1111;第一支撑板181的外侧面的前部为向着支架主体100倾斜设置的第一斜面183,第二支撑板182的外侧面的前部为向着支架主体100倾斜设置的第二斜面184;第一斜面183与其中一个前缩部斜面1111共面,第二斜面184与另一个前缩部斜面1111共面,以便于插入囊袋中。The outer side of the forward retraction structure 111 has two oppositely arranged front retraction inclined surfaces 1111; The front part of the outer side surface is a second inclined surface 184 inclined towards the bracket body 100; the first inclined surface 183 is coplanar with one of the inclined surfaces of the fore-reduction part 1111, and the second inclined surface 184 is coplanar with the other inclined surface of the fore-reduction part 1111, so as to facilitate the Insert into the pouch.

支撑杆200的中空通道210的前端上设有供前部定位器具连接的内连接部230。前部定位器具通过与内连接部230的连接,将支撑杆200的前端的位置固定,即前部定位器具顶住支撑杆200的前端。The front end of the hollow channel 210 of the support rod 200 is provided with an inner connecting part 230 for connecting the front positioning tool. The front positioning tool is connected with the inner connecting portion 230 to fix the position of the front end of the support rod 200 , that is, the front positioning tool presses against the front end of the support rod 200 .

本实施例中,内连接部230为内螺纹。前部定位器具为具有与内连接部230的内螺纹相应的外螺纹的医用定位器具。In this embodiment, the inner connecting portion 230 is an inner thread. The front positioning tool is a medical positioning tool having an external thread corresponding to the internal thread of the inner connecting portion 230 .

驱动部120上设有卡槽121。卡槽121可供推动驱动部120的医用工具卡入,便于推动驱动部120。The driving part 120 is provided with a card slot 121 . The clamping slot 121 can be inserted into the medical tool that pushes the driving part 120 , so as to facilitate the pushing of the driving part 120 .

本实施例中,驱动部120为圆柱形。该结构使得驱动部120能够被稳定地推动。In this embodiment, the driving portion 120 is cylindrical. This structure enables the driving part 120 to be pushed stably.

第一支撑板181和第二支撑板182结构相同,第一支撑板181的宽度W1能够提供较大的支撑面,稳定地支撑椎体。The first support plate 181 and the second support plate 182 have the same structure, and the width W1 of the first support plate 181 can provide a larger support surface and stably support the vertebral body.

每个前端辅助槽151的槽壁的前部设有前槽部前凹陷结构153,每个前端辅助槽151的槽壁的后部设有前槽部后凹陷结构154;每个后端辅助槽152的槽壁的前部设有后槽部前凹陷结构155,每个后端辅助槽152的槽壁的后部设有后槽部后凹陷结构156。The front part of the groove wall of each front end auxiliary groove 151 is provided with a front groove part front concave structure 153, and the rear part of the groove wall of each front end auxiliary groove 151 is provided with a front groove part rear concave structure 154; each rear auxiliary groove The front part of the groove wall of 152 is provided with a rear groove part front concave structure 155 , and the rear part of the groove wall of each rear end auxiliary groove 152 is provided with a rear groove part rear concave structure 156 .

前槽部前凹陷结构153包括两个相对设置于前端辅助槽151的槽壁的前部的第一前凹陷部,前槽部后凹陷结构154包括两个相对设置于前端辅助槽151的槽壁的后部的第一后凹陷部;后槽部前凹陷结构155包括两个相对设置于后端辅助槽152的槽壁的前部的第二前凹陷部;后槽部后凹陷结构156包括两个相对设置于后端辅助槽152的槽壁的后部的第二后凹陷部。The front recessed structure 153 of the front groove portion includes two first front recessed portions disposed opposite to the front of the groove wall of the front end auxiliary groove 151 , and the rear recessed structure 154 of the front groove portion includes two groove walls disposed opposite to the front end auxiliary groove 151 . The first rear recessed part of the rear part; the front recessed structure 155 of the rear groove part includes two second front recessed parts opposite to the front part of the groove wall of the rear end auxiliary groove 152; the rear recessed structure 156 of the rear groove part includes two a second rear concave part opposite to the rear part of the groove wall of the rear end auxiliary groove 152 .

本实施例的椎间融合器的使用方法,包括以下步骤:The method of using the intervertebral cage of the present embodiment includes the following steps:

1)将椎间融合器的药物吸附层20浸泡在骨形态发生蛋白或者干细胞中,使得所述药物吸附层20吸附骨形态发生蛋白或者干细胞;1) soaking the drug adsorption layer 20 of the interbody cage in bone morphogenetic protein or stem cells, so that the drug adsorption layer 20 adsorbs bone morphogenetic protein or stem cells;

2)当容纳部10达到椎体之间后,顶住支撑杆200的前端,推动驱动部120向着靠近安装部110的方向移动,支架主体100伸展为六边形结构,使容纳部10被撑开。2) When the accommodating part 10 reaches between the vertebral bodies, it pushes the front end of the support rod 200 and pushes the driving part 120 to move towards the direction close to the mounting part 110. The bracket body 100 is stretched into a hexagonal structure, so that the accommodating part 10 is supported. open.

实施例3Example 3

如图3、图14至图15所示,本实施例中,椎间融合器,还包括撑开部件300,所述撑开部件300为弹性板件,所述弹性板件卷曲回转形成由内至外依次环绕的多个圈层结构310,所有圈层结构310的中轴线共线。撑开部件300初始时,撑开部件300是收紧状态;当需要撑开部件300将容纳部10撑开时,驱动撑开部件300,使得撑开部件300处于舒展状态,则撑开部件300舒展为单个环绕圈层。As shown in FIGS. 3 , 14 to 15 , in this embodiment, the intervertebral cage further includes a spreading member 300 . The spreading member 300 is an elastic plate member, and the elastic plate member is curled and rotated to form an inner The central axes of all the ring structures 310 are collinear with respect to the plurality of ring structures 310 that are successively surrounded to the outside. When the opening part 300 is initially in a tightened state; when the opening part 300 needs to be opened to open the accommodating part 10, the opening part 300 is driven so that the opening part 300 is in a stretched state, then the opening part 300 is opened. Stretch into a single wraparound layer.

本实施例的椎间融合器的使用方法,包括以下步骤:The method of using the intervertebral cage of the present embodiment includes the following steps:

1)将椎间融合器的药物吸附层20浸泡在骨形态发生蛋白或者干细胞中,使得所述药物吸附层20吸附骨形态发生蛋白或者干细胞;1) soaking the drug adsorption layer 20 of the interbody cage in bone morphogenetic protein or stem cells, so that the drug adsorption layer 20 adsorbs bone morphogenetic protein or stem cells;

2)当容纳部10达到椎体之间后,驱动撑开部件300,使得撑开部件300舒展,撑开部件300舒展为单个环绕圈层,撑开部件300将容纳部10撑开。2) After the accommodating part 10 reaches between the vertebral bodies, the spreading member 300 is driven, so that the spreading member 300 is stretched.

综上,本发明有效克服了现有技术中的种种缺点而具高度产业利用价值。To sum up, the present invention effectively overcomes various shortcomings in the prior art and has high industrial utilization value.

上述实施例仅例示性说明本发明的原理及其功效,而非用于限制本发明。任何熟悉此技术的人士皆可在不违背本发明的精神及范畴下,对上述实施例进行修饰或改变。因此,举凡所属技术领域中具有通常知识者在未脱离本发明所揭示的精神与技术思想下所完成的一切等效修饰或改变,仍应由本发明的权利要求所涵盖。The above-mentioned embodiments merely illustrate the principles and effects of the present invention, but are not intended to limit the present invention. Anyone skilled in the art can make modifications or changes to the above embodiments without departing from the spirit and scope of the present invention. Therefore, all equivalent modifications or changes made by those with ordinary knowledge in the technical field without departing from the spirit and technical idea disclosed in the present invention should still be covered by the claims of the present invention.

Claims (10)

1.一种椎间融合器,其特征在于,包括:容纳部(10),所述容纳部(10)可撑开,所述容纳部(10)上设有开口(11),所述容纳部(10)的外侧面上包覆有药物吸附层(20)。1. An intervertebral cage, characterized in that it comprises: an accommodating part (10), the accommodating part (10) can be stretched, an opening (11) is provided on the accommodating part (10), the accommodating part (10) is The outer surface of the part (10) is covered with a drug adsorption layer (20). 2.根据权利要求1所述的椎间融合器,其特征在于:所述药物吸附层(20)的材料为医用凝胶。2 . The interbody cage according to claim 1 , wherein the material of the drug adsorption layer ( 20 ) is medical gel. 3 . 3.根据权利要求3所述的椎间融合器,其特征在于:所述药物吸附层(20)所吸附的药物为能够吸附促进骨生长的物质。3 . The cage according to claim 3 , wherein the drug adsorbed by the drug adsorption layer ( 20 ) is a substance capable of adsorbing and promoting bone growth. 4 . 4.一种椎间融合器,其特征在于,包括:容纳部(10),所述容纳部(10)可撑开,所述容纳部(10)上设有开口(11),所述容纳部(10)的外侧面上包覆有药物吸附层(20),所述药物吸附层(20)的材料为医用凝胶;所述药物吸附层(20)所吸附的药物为能够吸附促进骨生长的物质。4. An intervertebral cage, characterized in that it comprises: an accommodating part (10), the accommodating part (10) can be stretched, an opening (11) is provided on the accommodating part (10), the accommodating part (10) is The outer surface of the part (10) is covered with a drug adsorption layer (20), and the material of the drug adsorption layer (20) is medical gel; the drug adsorbed by the drug adsorption layer (20) is capable of adsorbing and promoting bone growing substance. 5.根据权利要求1-4中任意一项所述的椎间融合器,其特征在于:所述药物吸附层(20)所吸附的药物为骨形态发生蛋白或者干细胞。5. The interbody cage according to any one of claims 1-4, wherein the drug adsorbed by the drug adsorption layer (20) is bone morphogenetic protein or stem cells. 6.根据权利要求1或4所述的椎间融合器,其特征在于:所述容纳部(10)为囊袋。6. The intervertebral cage according to claim 1 or 4, characterized in that: the accommodating part (10) is a pouch. 7.根据权利要求1或4所述的椎间融合器,其特征在于:还包括连接杆(30),所述连接杆(30)的一端与所述开口(11)连接,沿着所述连接杆(30)的轴向设有中间通孔(31),所述中间通孔(31)与所述开口(11)连通。7. The intervertebral cage according to claim 1 or 4, characterized in that it further comprises a connecting rod (30), one end of the connecting rod (30) is connected with the opening (11), along the An intermediate through hole (31) is provided in the axial direction of the connecting rod (30), and the intermediate through hole (31) communicates with the opening (11). 8.根据权利要求1或4所述的椎间融合器,其特征在于:还包括撑开支架,所述撑开支架可插入于所述容纳部(10)中;所述撑开支架包括:支架主体(100)和支撑杆(200);所述支架主体(100)为长条状结构,所述支架主体(100)的外周侧面包括依次连接的第一开槽面(101)、第一支撑面(102)、第二开槽面(103)和第二支撑面(104);所述第一开槽面(101)与所述第二开槽面(103)相对设置;所述第一支撑面(102)与所述第二支撑面(104)相对设置;8. The intervertebral cage according to claim 1 or 4, characterized in that it further comprises a spreader bracket, which can be inserted into the accommodating part (10); the spreader bracket comprises: A bracket main body (100) and a support rod (200); the bracket main body (100) is a long strip structure, and the outer peripheral side surface of the bracket main body (100) comprises a first slotted surface (101), a first slotted surface (101), a first a support surface (102), a second slotted surface (103) and a second support surface (104); the first slotted surface (101) is arranged opposite to the second slotted surface (103); the first slotted surface (101) is arranged opposite to the second slotted surface (103); A support surface (102) is arranged opposite to the second support surface (104); 所述支架主体(100)在长度方向上的前端上设有安装部(110),所述支架主体(100)在长度方向上的后端上设有驱动部(120);The front end of the bracket body (100) in the longitudinal direction is provided with a mounting part (110), and the rear end of the bracket body (100) in the longitudinal direction is provided with a driving part (120); 所述支架主体(100)上设有贯通孔(130),所述贯通孔(130)的两端分别贯通至所述安装部(110)的前端和所述驱动部(120)的后端,所述贯通孔(130)的轴向与所述支架主体(100)的长度方向同向;The bracket body (100) is provided with a through hole (130), and both ends of the through hole (130) respectively penetrate to the front end of the mounting portion (110) and the rear end of the driving portion (120), The axial direction of the through hole (130) is the same as the longitudinal direction of the bracket body (100); 所述支撑杆(200)依次穿过所述安装部(110)、所述支架主体(100)和所述驱动部(120),所述支撑杆(200)与所述贯通孔(130)为间隙配合,所述支撑杆(200)与所述安装部(110)固定连接;所述支撑杆(200)具有中空通道(210),所述中空通道(210)贯通至所述支撑杆(200)的后端;The support rod (200) passes through the mounting part (110), the bracket main body (100) and the driving part (120) in sequence, and the support rod (200) and the through hole (130) are In clearance fit, the support rod (200) is fixedly connected with the mounting portion (110); the support rod (200) has a hollow channel (210), and the hollow channel (210) penetrates to the support rod (200). ) backend; 在所述第一开槽面(101)上的宽度方向上的中部具有中间长条槽(140),所述中间长条槽(140)贯通至所述第二开槽面(103),所述中间长条槽(140)的长度方向与所述第一开槽面(101)的长度方向同向;There is a middle elongated groove (140) in the middle part in the width direction on the first slotted surface (101), and the middle elongated slot (140) penetrates to the second slotted surface (103), so The length direction of the middle elongated groove (140) is the same as the length direction of the first slotted surface (101); 沿着所述第一开槽面(101)上的宽度方向,在所述中间长条槽(140)的两侧分别设有第一辅助槽组(150)和第二辅助槽组(160);所述第一辅助槽组(150)和所述第二辅助槽组(160)的结构相同,所述第一辅助槽组(150)包括沿着所述第一开槽面(101)上的长度方向依次设置的前端辅助槽(151)和后端辅助槽(152),所述前端辅助槽(151)和所述后端辅助槽(152)之间具有间隔,所述前端辅助槽(151)的后端与所述后端辅助槽(152)的前端之间的连线的中点连接所述中间长条槽(140)的长度的中点的连线与所述支架主体(100)的宽度方向同向;A first auxiliary groove group (150) and a second auxiliary groove group (160) are respectively provided on both sides of the middle elongated groove (140) along the width direction of the first grooved surface (101) ; The structure of the first auxiliary groove group (150) and the second auxiliary groove group (160) are the same, and the first auxiliary groove group (150) includes a groove along the first grooved surface (101) A front-end auxiliary groove (151) and a rear-end auxiliary groove (152) are arranged in sequence in the length direction of the front-end auxiliary groove (151) and there is a space between the front-end auxiliary groove (151) and the rear-end auxiliary groove (152), and the front-end auxiliary groove ( 151) and the front end of the rear auxiliary groove (152), the midpoint of the line connecting the midpoint of the length of the middle elongated groove (140) and the bracket main body (100) ) in the same width direction; 所述第一支撑面(102)通过第一连接块(171)与第一支撑板(181)连接;所述第二支撑面(104)通过第二连接块(172)与第二支撑板(182)连接;The first support surface (102) is connected to the first support plate (181) through the first connection block (171); the second support surface (104) is connected to the second support plate (181) through the second connection block (172). 182) connect; 所述支撑杆(200)的外侧壁上具有侧壁通孔(220),所述侧壁通孔(220)与所述中空通道(210)连通,所述侧壁通孔(220)处于所述贯通孔(130)与所述中间长条槽(140)连通所构成的主腔室中,且将所述支架主体(100)的前端和后端相比较,所述侧壁通孔(220)较靠近所述支架主体(100)的前端;The outer side wall of the support rod (200) is provided with a side wall through hole (220), the side wall through hole (220) communicates with the hollow channel (210), and the side wall through hole (220) is located at the In the main chamber formed by the communication between the through hole (130) and the middle elongated groove (140), and comparing the front end and the rear end of the bracket body (100), the side wall through hole (220) ) is closer to the front end of the bracket body (100); 顶住所述支撑杆(200)的前端,推动所述驱动部(120)向着靠近所述安装部(110)的方向移动,所述支架主体(100)伸展为六边形结构。The front end of the support rod (200) is pushed against the driving part (120) to move toward the direction close to the installation part (110), and the bracket body (100) extends into a hexagonal structure. 9.根据权利要求1或4所述的椎间融合器,其特征在于:还包括撑开部件(300),所述撑开部件(300)为弹性板件,所述弹性板件卷曲回转形成由内至外依次环绕的多个圈层结构(310),所有圈层结构(310)的中轴线共线。9. The intervertebral cage according to claim 1 or 4, characterized in that: further comprising a spreading member (300), the spreading member (300) is an elastic plate member, and the elastic plate member is formed by curling and turning For a plurality of ring-layer structures (310) that are sequentially surrounded from inside to outside, the central axes of all the ring-layer structures (310) are collinear. 10.一种椎间融合器的使用方法,其特征在于:将权利要求1或4中所述的椎间融合器的药物吸附层(20)浸泡在骨形态发生蛋白或者干细胞中,使得所述药物吸附层(20)吸附骨形态发生蛋白或者干细胞。10. A method of using an intervertebral cage, characterized in that: the drug-adsorbing layer (20) of the intervertebral cage according to claim 1 or 4 is soaked in bone morphogenetic protein or stem cells, so that the The drug adsorption layer (20) adsorbs bone morphogenetic proteins or stem cells.
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Publication number Priority date Publication date Assignee Title
CN115531055A (en) * 2020-10-22 2022-12-30 上海三友医疗器械股份有限公司 Interbody fusion cage and method of use

Citations (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5102402A (en) * 1991-01-04 1992-04-07 Medtronic, Inc. Releasable coatings on balloon catheters
CN1708327A (en) * 2002-10-30 2005-12-14 生物休眠有限公司 Device with an expandable portion for drug release
CN101052427A (en) * 2004-10-06 2007-10-10 拜克技术有限公司 Transparent hyaluronic acid coated bone implanting appliance
CN101130112A (en) * 2002-09-20 2008-02-27 乌尔里希·施佩克 Balloon catheter for drug delivery, method of making and use thereof
CN201168075Y (en) * 2008-03-21 2008-12-24 杨惠林 Minimal invasion intervertebral fusion device
CN101969888A (en) * 2008-01-16 2011-02-09 华沙整形外科股份有限公司 Joint replacement device
CN102038563A (en) * 2003-10-22 2011-05-04 先锋外科技术公司 Artificial intervertebral disc device
CN102341066A (en) * 2008-12-31 2012-02-01 奥马尔·F·希门尼斯 Method and apparatus for vertebral body distraction and fusion using curved members
CN102596109A (en) * 2009-09-17 2012-07-18 斯恩蒂斯有限公司 Intervertebral implant having extendable bone fixation members
CN103610523A (en) * 2013-12-18 2014-03-05 广州聚生生物科技有限公司 Minimally invasive lateral approach interbody fusion device
CN105611900A (en) * 2013-10-07 2016-05-25 华沙整形外科股份有限公司 Spinal implant system and method for lumbar and lumbosacral fusion
CN106726019A (en) * 2017-02-06 2017-05-31 南京市第医院 The minimally invasive fusion device of intervertebral spinal fusion nanometer biological glass coating
CN107920846A (en) * 2015-08-30 2018-04-17 摩根·帕卡德·洛里奥 Expandable intervertebral fusion device with living hinge, system and method of manufacture
CN108135710A (en) * 2015-10-16 2018-06-08 华沙整形外科股份有限公司 Expandable intervertebral implant system and method
CN115531055A (en) * 2020-10-22 2022-12-30 上海三友医疗器械股份有限公司 Interbody fusion cage and method of use

Patent Citations (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5102402A (en) * 1991-01-04 1992-04-07 Medtronic, Inc. Releasable coatings on balloon catheters
CN101130112A (en) * 2002-09-20 2008-02-27 乌尔里希·施佩克 Balloon catheter for drug delivery, method of making and use thereof
CN1708327A (en) * 2002-10-30 2005-12-14 生物休眠有限公司 Device with an expandable portion for drug release
CN102038563A (en) * 2003-10-22 2011-05-04 先锋外科技术公司 Artificial intervertebral disc device
CN101052427A (en) * 2004-10-06 2007-10-10 拜克技术有限公司 Transparent hyaluronic acid coated bone implanting appliance
CN101969888A (en) * 2008-01-16 2011-02-09 华沙整形外科股份有限公司 Joint replacement device
CN201168075Y (en) * 2008-03-21 2008-12-24 杨惠林 Minimal invasion intervertebral fusion device
CN102341066A (en) * 2008-12-31 2012-02-01 奥马尔·F·希门尼斯 Method and apparatus for vertebral body distraction and fusion using curved members
CN102596109A (en) * 2009-09-17 2012-07-18 斯恩蒂斯有限公司 Intervertebral implant having extendable bone fixation members
CN105611900A (en) * 2013-10-07 2016-05-25 华沙整形外科股份有限公司 Spinal implant system and method for lumbar and lumbosacral fusion
CN103610523A (en) * 2013-12-18 2014-03-05 广州聚生生物科技有限公司 Minimally invasive lateral approach interbody fusion device
CN107920846A (en) * 2015-08-30 2018-04-17 摩根·帕卡德·洛里奥 Expandable intervertebral fusion device with living hinge, system and method of manufacture
CN108135710A (en) * 2015-10-16 2018-06-08 华沙整形外科股份有限公司 Expandable intervertebral implant system and method
CN106726019A (en) * 2017-02-06 2017-05-31 南京市第医院 The minimally invasive fusion device of intervertebral spinal fusion nanometer biological glass coating
CN115531055A (en) * 2020-10-22 2022-12-30 上海三友医疗器械股份有限公司 Interbody fusion cage and method of use

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