CN108113782A - Vertebral body fusion cage - Google Patents
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- CN108113782A CN108113782A CN201711322705.5A CN201711322705A CN108113782A CN 108113782 A CN108113782 A CN 108113782A CN 201711322705 A CN201711322705 A CN 201711322705A CN 108113782 A CN108113782 A CN 108113782A
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- 230000004927 fusion Effects 0.000 title claims abstract description 39
- 238000001125 extrusion Methods 0.000 claims description 16
- 230000006378 damage Effects 0.000 abstract description 11
- 208000027418 Wounds and injury Diseases 0.000 abstract description 3
- 208000014674 injury Diseases 0.000 abstract 1
- 210000000988 bone and bone Anatomy 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- 238000010586 diagram Methods 0.000 description 4
- 230000035876 healing Effects 0.000 description 3
- 206010052428 Wound Diseases 0.000 description 2
- 238000002513 implantation Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 206010017076 Fracture Diseases 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 239000004696 Poly ether ether ketone Substances 0.000 description 1
- 208000002847 Surgical Wound Diseases 0.000 description 1
- 229910001069 Ti alloy Inorganic materials 0.000 description 1
- JUPQTSLXMOCDHR-UHFFFAOYSA-N benzene-1,4-diol;bis(4-fluorophenyl)methanone Chemical compound OC1=CC=C(O)C=C1.C1=CC(F)=CC=C1C(=O)C1=CC=C(F)C=C1 JUPQTSLXMOCDHR-UHFFFAOYSA-N 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000003412 degenerative effect Effects 0.000 description 1
- 230000014509 gene expression Effects 0.000 description 1
- 239000007943 implant Substances 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 230000003902 lesion Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
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- 239000002103 nanocoating Substances 0.000 description 1
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- 229920002530 polyetherether ketone Polymers 0.000 description 1
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS 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
- A61F2/00—Filters 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
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/44—Joints for the spine, e.g. vertebrae, spinal discs
- A61F2/4455—Joints 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
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Abstract
Description
技术领域technical field
本发明涉及医疗器械领域,特别涉及一种椎体融合器。The invention relates to the field of medical instruments, in particular to a vertebral body fusion device.
背景技术Background technique
在日常生活中,由于肿瘤、骨折、感染、退行性病变等原因导致椎体损坏的病例时有发生,在治疗这些患者时,采用的方式是在损坏的椎体间植入一个融合器,使骨组织产生爬行替代,从而修复损坏的椎体,然而传统的椎体融合器大多外型较大,使得手术切口也很大,而一般外型较小椎体融合器,容易造成椎体终板损伤,因此均对患者身体造成较大损伤,影响治愈成功率。In daily life, cases of vertebral body damage due to tumors, fractures, infections, degenerative lesions and other reasons occur from time to time. When treating these patients, the method used is to implant a fusion device between the damaged vertebral bodies. The bone tissue crawls and replaces, thereby repairing the damaged vertebral body. However, most of the traditional vertebral body fusion devices are large in size, which makes the surgical incision also large. Therefore, they all cause greater damage to the patient's body and affect the success rate of healing.
发明内容Contents of the invention
基于此,本发明在于克服现有技术的缺陷,提供一种椎体融合器,可在手术过程中减少对骨骼的损伤并能有效避免刺穿患者椎体终板,从而减少对患者身体的损伤。Based on this, the present invention overcomes the defects of the prior art and provides a vertebral body fusion device, which can reduce the damage to the bone during the operation and can effectively avoid piercing the patient's vertebral body endplate, thereby reducing the damage to the patient's body .
一种椎体融合器,包括可膨胀管,所述可膨胀管上开设有间隔设置的多个第一缺口,相邻两个第一缺口之间的管壁形成撑起部,所述撑起部的侧部设有延伸部,所述可膨胀管能被挤压膨胀,膨胀状态时,所述撑起部及延伸部向外变形凸起。A vertebral body fusion device, comprising an expandable tube, the expandable tube is provided with a plurality of first gaps arranged at intervals, and the tube wall between two adjacent first gaps forms a propping part, and the propping up The side part of the tube is provided with an extension part, and the expandable tube can be squeezed and expanded. When in an expanded state, the propping part and the extension part deform and protrude outward.
使用时,通过变形工具将未变形的椎体融合器由顶端至底端逐渐植入椎体间,然后通过变形工具对可膨胀管的底端进行挤压,由于所述撑起部的侧部设有延伸部,使可膨胀管的撑起部沿延伸部的两侧向外变形凸起,而与延伸部对应的撑起部为变形后的最高点,最高点处的撑起部与延伸部一起,形成用于支撑椎体终板的支撑面,增大与椎体终板的接触面积,提高支撑的稳定性,确保支撑高度的调节及强度,避免支撑部最高点凸起刺穿椎体终板,对患者身体造成损伤,有效保证治愈成功率。而且该椎体融合器,结构简单,变形前体积小,可在手术过程中减少对骨骼的损伤,患者需要切口的植入伤口小,对患者损伤较小。When in use, the undeformed vertebral body fusion device is gradually implanted between the vertebral bodies from the top to the bottom through the deformation tool, and then the bottom end of the expandable tube is squeezed through the deformation tool, because the side of the propping part There is an extension part, so that the propping part of the expandable tube is deformed and protruded outward along both sides of the extension part, and the propping part corresponding to the extension part is the highest point after deformation, and the propping part at the highest point is connected with the extension part. Together, they form a support surface for supporting the endplate of the vertebral body, increase the contact area with the endplate of the vertebral body, improve the stability of the support, ensure the adjustment and strength of the support height, and avoid the protrusion of the highest point of the support part from piercing the vertebral body. The body endplate, which causes damage to the patient's body, effectively guarantees the success rate of healing. Moreover, the vertebral body fusion device has a simple structure and a small volume before deformation, which can reduce damage to the bone during the operation, and the implantation wound of the patient requiring an incision is small, and the damage to the patient is small.
进一步地,所述延伸部的两侧开设有凹口,膨胀状态时,所述撑起部沿所述凹口向外变形凸起。Further, notches are formed on both sides of the extension part, and in the expanded state, the propping part deforms and protrudes outward along the notches.
进一步地,所述可膨胀管上沿轴向方向间隔设有两列所述第一缺口,两列第一缺口相对设置,相邻列的第一缺口之间的管壁形成所述撑起部。Further, the expandable tube is provided with two rows of first notches at intervals along the axial direction, and the two rows of first notches are oppositely arranged, and the tube wall between the first notches of adjacent rows forms the propping portion .
进一步地,所述可膨胀管上还开设有四列沿轴向方向布置的第二缺口,四列所述第二缺口绕可膨胀管的周向间隔设置,相邻列的第二缺口之间的管壁形成抗旋部,膨胀状态时,所述抗旋部向外变形凸起。Further, the expandable tube is also provided with four rows of second gaps arranged in the axial direction, and the four rows of second gaps are arranged at intervals around the circumference of the expandable tube. The pipe wall of the pipe forms an anti-rotation part, and when in an expanded state, the anti-rotation part deforms and protrudes outward.
进一步地,其中一列所述撑起部位于其中两列所述抗旋部之间,另一列撑起部位于另外两列抗旋部之间,且膨胀状态时,所述撑起部的最高点与所述抗旋部的最高点平齐。Further, one row of propping parts is located between two rows of anti-rotation parts, the other row of propping parts is located between the other two rows of anti-rotation parts, and in the expanded state, the highest point of the propping parts flush with the highest point of the anti-rotation section.
进一步地,四列所述第二缺口绕可膨胀管的周向均匀间隔设置;或者其中两列所述第二缺口相对设置,另外两列所述第二缺口相对设置。Further, four rows of the second notches are evenly spaced around the circumference of the expandable tube; or two rows of the second notches are oppositely arranged, and the other two rows of the second notches are oppositely arranged.
进一步地,所述抗旋部的中部开设有挤压口。Further, an extrusion opening is opened in the middle of the anti-rotation part.
进一步地,所述第二缺口开设在所述可膨胀管两端;或者在轴向方向上,所述第二缺口与第一缺口交替设置。Further, the second notches are provided at both ends of the expandable tube; or in the axial direction, the second notches are arranged alternately with the first notches.
进一步地,所述第一缺口的两端均设有第一限位片,两个第一限位片之间留有挤压间隔,所述第二缺口的两端均设有第二限位片,两个第二限位片之间留有挤压间隔。Further, both ends of the first notch are provided with first limiting pieces, and there is an extrusion space between the two first limiting pieces, and both ends of the second notch are provided with second limiting pieces. sheet, and there is an extrusion interval between the two second limiting sheets.
进一步地,所述的椎体融合器还包括内芯,所述内芯设置在所述可膨胀管内,且所述可膨胀管的顶端与所述内芯的顶端连接,所述内芯的底端设有与变形工具匹配的螺纹。Further, the vertebral body fusion device also includes an inner core, the inner core is arranged in the expandable tube, and the top end of the expandable tube is connected to the top end of the inner core, and the bottom of the inner core The end is threaded to match the deformation tool.
附图说明Description of drawings
图1为本发明一实施例所述椎体融合器未变形时的结构示意图;Fig. 1 is a schematic structural view of the undeformed vertebral body fusion device according to an embodiment of the present invention;
图2为图1所示椎体融合器中的可膨胀管的结构示意图;Fig. 2 is a structural schematic diagram of the expandable tube in the vertebral body fusion device shown in Fig. 1;
图3为图1所示椎体融合器中的内芯的结构示意图;Fig. 3 is a structural schematic diagram of the inner core in the vertebral fusion device shown in Fig. 1;
图4为图1所示椎体融合器膨胀状态时的结构示意图;Fig. 4 is a structural schematic view of the expanded state of the vertebral body fusion device shown in Fig. 1;
图5为图4所示椎体融合器中的可膨胀管的结构示意图;Fig. 5 is a structural schematic diagram of the expandable tube in the vertebral body fusion device shown in Fig. 4;
图6为本发明另一实施例所述椎体融合器未变形时的结构示意图;Fig. 6 is a schematic structural view of the undeformed vertebral body fusion device according to another embodiment of the present invention;
图7为图6所示椎体融合器中的可膨胀管的结构示意图;Fig. 7 is a structural schematic diagram of the expandable tube in the vertebral body fusion device shown in Fig. 6;
图8为图6所示椎体融合器膨胀状态时的结构示意图;Fig. 8 is a structural schematic view of the expanded state of the vertebral fusion cage shown in Fig. 6;
图9为图8所示椎体融合器中的可膨胀管的结构示意图。Fig. 9 is a schematic structural view of the expandable tube in the vertebral fusion cage shown in Fig. 8 .
附图标记说明:Explanation of reference signs:
10、可膨胀管,110、第一缺口,112、第一限位片,120、撑起部,130、延伸部,132、凹口,140、第二缺口,142、第二限位片,150、抗旋部,152、挤压口,20、内芯,210、连扳。10. Expandable tube, 110, first notch, 112, first limiting piece, 120, propping part, 130, extension part, 132, notch, 140, second notch, 142, second limiting piece, 150, anti-rotation portion, 152, extrusion mouth, 20, inner core, 210, even pull.
具体实施方式Detailed ways
为了便于理解本发明,下面将参照相关附图对本发明进行更全面的描述。附图中给出了本发明的较佳实施方式。但是,本发明可以以许多不同的形式来实现,并不限于本文所描述的实施方式。相反地,提供这些实施方式的目的是使对本发明的公开内容理解的更加透彻全面。In order to facilitate the understanding of the present invention, the present invention will be described more fully below with reference to the associated drawings. Preferred embodiments of the invention are shown in the accompanying drawings. However, the present invention can be embodied in many different forms and is not limited to the embodiments described herein. On the contrary, the purpose of providing these embodiments is to make the disclosure of the present invention more thorough and comprehensive.
需要说明的是,当元件被称为“固定于”另一个元件,它可以直接在另一个元件上或者也可以存在居中的元件。当一个元件被认为是“连接”另一个元件,它可以是直接连接到另一个元件或者可能同时存在居中元件。相反,当元件被称作“直接在”另一元件“上”时,不存在中间元件。本文所使用的术语“垂直的”、“水平的”、“左”、“右”以及类似的表述只是为了说明的目的,并不表示是唯一的实施方式。It should be noted that when an element is referred to as being “fixed” to another element, it can be directly on the other element or there can also be an intervening element. When an element is referred to as being "connected to" another element, it can be directly connected to the other element or intervening elements may also be present. In contrast, when an element is referred to as being "directly on" another element, there are no intervening elements present. The terms "vertical," "horizontal," "left," "right," and similar expressions are used herein for purposes of illustration only and are not intended to represent the only embodiments.
除非另有定义,本文所使用的所有的技术和科学术语与属于本发明的技术领域的技术人员通常理解的含义相同。本文中在本发明的说明书中所使用的术语只是为了描述具体的实施方式的目的,不是旨在于限制本发明。本文所使用的术语“及/或”包括一个或多个相关的所列项目的任意的和所有的组合。Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the technical field of the invention. The terminology used herein in the description of the present invention is only for the purpose of describing specific embodiments, and is not intended to limit the present invention. As used herein, the term "and/or" includes any and all combinations of one or more of the associated listed items.
如图1-5所示,一实施例提供一种椎体融合器,包括可膨胀管10,所述可膨胀管10上开设有间隔设置的多个第一缺口110,相邻两个第一缺口110之间的管壁形成撑起部120,所述撑起部120的侧部设有延伸部130,所述可膨胀管10能被挤压膨胀,膨胀状态时,所述撑起部120及延伸部130向外变形凸起。As shown in Figures 1-5, an embodiment provides a vertebral body fusion device, which includes an expandable tube 10, and a plurality of first notches 110 arranged at intervals are opened on the expandable tube 10, and two adjacent first notches 110 are provided. The tube wall between the gaps 110 forms a propping part 120, and the side of the propping part 120 is provided with an extension part 130, and the expandable tube 10 can be squeezed and expanded. When in an expanded state, the propping part 120 And the extension part 130 deforms and protrudes outward.
使用时,通过变形工具将未变形的椎体融合器由顶端至底端逐渐植入椎体间,然后通过变形工具对可膨胀管10的底端进行挤压,由于所述撑起部120的侧部设有延伸部130,使可膨胀管10的撑起部120沿延伸部130的两侧向外变形凸起,而与延伸部130对应的撑起部120为变形后的最高点,增大椎体融合器轴向方向与椎体终板的接触面积,同时由于延伸部130位于最高点撑起部120的侧部,增大了椎体融合器径向方向与椎体终板的接触面积,从而最高点处的撑起部120与延伸部130一起,形成用于支撑椎体终板的支撑面,使与椎体终板接触的面积从径向与轴向均增大,不仅提高支撑的稳定性,确保支撑高度的调节及强度,避免支撑部最高点凸起刺穿椎体终板,对患者身体造成损伤,有效保证治愈成功率。而且该椎体融合器,结构简单,变形前体积小,可在手术过程中减少对骨骼的损伤,患者需要切口的植入伤口小,对患者损伤较小。变形后的椎体融合器,内部植骨空间更大,愈合成功率更高。所述延伸部130由第一缺口110内的可膨胀管10的管壁切割形成。When in use, the undeformed vertebral body fusion device is gradually implanted between the vertebral bodies from the top end to the bottom end through the deformation tool, and then the bottom end of the expandable tube 10 is squeezed through the deformation tool, due to the support portion 120 The side part is provided with an extension part 130, so that the propping part 120 of the expandable tube 10 deforms and protrudes outward along both sides of the extension part 130, and the propping part 120 corresponding to the extension part 130 is the highest point after deformation, increasing The contact area between the large vertebral body fusion cage and the vertebral body endplate in the axial direction, and because the extension part 130 is located on the side of the highest point support part 120, the contact area between the vertebral body fusion cage and the vertebral body endplate in the radial direction is increased area, so that the supporting part 120 and the extension part 130 at the highest point form a supporting surface for supporting the endplate of the vertebral body, so that the area in contact with the endplate of the vertebral body increases from both radial and axial directions, which not only improves The stability of the support ensures the adjustment and strength of the support height, avoids the highest point of the support part from piercing the vertebral endplate, causing damage to the patient's body, and effectively guarantees the success rate of the cure. Moreover, the vertebral body fusion device has a simple structure and a small volume before deformation, which can reduce damage to the bone during the operation, and the implantation wound of the patient requiring an incision is small, and the damage to the patient is small. The deformed vertebral body fusion cage has a larger internal space for bone grafting and a higher healing rate. The extension part 130 is formed by cutting the tube wall of the expandable tube 10 in the first gap 110 .
进一步地,如图1、2所示,所述延伸部130的两侧开设有凹口132,膨胀状态时,所述撑起部120沿所述凹口132向外变形凸起。当可膨胀管10受挤压时,所述凹口132处强度较撑开部其他地方小,撑起部120能沿凹口132处向外膨胀变形,确保两凹口132之间的撑起部120为变形后的最高点,从而与延伸部130一起形成支撑面,增大与椎体终板的接触面积。Further, as shown in FIGS. 1 and 2 , notches 132 are formed on both sides of the extension part 130 , and in the expanded state, the propping part 120 deforms and protrudes outward along the notches 132 . When the expandable tube 10 is squeezed, the strength of the notch 132 is smaller than that of other parts of the stretching part, and the propping part 120 can expand and deform outward along the notch 132 to ensure the propping up between the two notches 132 The part 120 is the highest point after deformation, so as to form a support surface together with the extension part 130, and increase the contact area with the endplate of the vertebral body.
具体地,如图1-4所示,本实施例所述可膨胀管10上沿轴向方向间隔设有两列所述第一缺口110,两列第一缺口110相对设置,相邻列的第一缺口110之间的管壁形成所述撑起部120。即两列撑起部120变形后形成相对设置的两列凸起,每列中的凸起间隔布置,分别用于对椎体终板的上板与下板进行支撑。Specifically, as shown in Figures 1-4, the expandable tube 10 of this embodiment is provided with two rows of first notches 110 at intervals along the axial direction, and the two rows of first notches 110 are arranged opposite to each other. The tube wall between the first gaps 110 forms the propping portion 120 . That is, the two rows of propping parts 120 are deformed to form two rows of projections that are oppositely arranged, and the projections in each row are arranged at intervals to support the upper plate and the lower plate of the endplate of the vertebral body respectively.
进一步地,所述可膨胀管10上还开设有四列沿轴向方向布置的第二缺口140,四列所述第二缺口140绕可膨胀管10的周向间隔设置,相邻列的第二缺口140之间的管壁形成抗旋部150,膨胀状态时,所述抗旋部150向外变形凸起。当可膨胀管10被挤压变形时,四列抗旋部150向外膨胀变形,从可膨胀管10的一端向另一端看,四列抗旋部150形成十字状,一方面能起到支撑椎体终板的作用,另一方面避免可膨胀管10旋转,使可膨胀管10的两个撑起部120能稳固地顶起椎体终板。Further, the expandable tube 10 is also provided with four rows of second notches 140 arranged in the axial direction, the four rows of second notches 140 are arranged at intervals around the circumference of the expandable tube 10 , and the first notches 140 of adjacent rows The tube wall between the two notches 140 forms an anti-rotation portion 150 , and when in an expanded state, the anti-rotation portion 150 deforms and protrudes outward. When the expandable tube 10 is squeezed and deformed, the four rows of anti-rotation parts 150 expand and deform outwards. Viewed from one end of the expandable tube 10 to the other end, the four rows of anti-rotation parts 150 form a cross shape, which can play a supporting role on the one hand. The role of the endplate of the vertebral body, on the other hand, prevents the expandable tube 10 from rotating, so that the two propping parts 120 of the expandable tube 10 can firmly lift up the endplate of the vertebral body.
进一步地,其中一列所述撑起部120位于其中两列所述抗旋部150之间,另一列撑起部120位于另外两列抗旋部150之间,且膨胀状态时,所述撑起部120的最高点与所述抗旋部150的最高点平齐。变形后的其中两列抗旋部150支撑在椎体终板的下板上,另外两列抗旋部150支撑在椎体终板的上板上。可选的,四列所述第二缺口140绕可膨胀管10的周向均匀间隔设置,即四列抗旋部150绕可膨胀管10的周向均匀布置,变形后相邻的抗旋部150之间呈90°夹角;或者其中两列所述第二缺口140相对设置,另外两列所述第二缺口140相对设置,即四列抗旋部150的其中两列相对设置,另外两列相对设置,形成上下对应的支撑。Further, one row of propping parts 120 is located between two rows of anti-rotation parts 150, and the other row of propping parts 120 is located between the other two rows of anti-rotation parts 150. The highest point of the portion 120 is flush with the highest point of the anti-rotation portion 150 . After deformation, two rows of anti-rotation parts 150 are supported on the lower plate of the vertebral endplate, and the other two rows of anti-rotation parts 150 are supported on the upper plate of the vertebral body endplate. Optionally, the four rows of the second notches 140 are evenly spaced around the circumference of the expandable tube 10, that is, the four rows of anti-rotation parts 150 are evenly arranged around the circumference of the expandable tube 10, and the adjacent anti-rotation parts after deformation 150 are at an angle of 90°; or two rows of the second notches 140 are arranged oppositely, and the other two rows of the second notches 140 are arranged oppositely, that is, two rows of the four rows of anti-rotation parts 150 are arranged oppositely, and the other two rows of the second notches 140 are arranged oppositely. The columns are set relative to each other to form support corresponding to the upper and lower sides.
进一步地,如图1、2、6、7所示,所述抗旋部150的中部开设有挤压口152。所述挤压口152由抗旋部150两侧的中部凹陷切割形成,挤压口152处的强度小于抗旋部150其他处的强度,挤压过程中便于沿挤压口152处向外变形凸起。Further, as shown in FIGS. 1 , 2 , 6 and 7 , an extrusion opening 152 is opened in the middle of the anti-rotation portion 150 . The extrusion opening 152 is formed by cutting the middle part of the anti-rotation part 150. The strength of the extrusion opening 152 is lower than that of other parts of the anti-rotation part 150, and it is easy to deform outward along the extrusion opening 152 during the extrusion process. raised.
进一步地,所述第一缺口110的两端均设有第一限位片112,对应两个第一限位片112之间留有挤压间隔,所述第二缺口140的两端均设有第二限位片142,对应两个第二限位片142之间留有挤压间隔。膨胀状态时,由于可膨胀管10被压缩变形,对应两个第一限位片112、对应两个第二限位片142逐步靠拢直至相互抵接,此时可膨胀管10不能再被挤压变形。可选的,也可只在第一缺口110的一端设置第一限位片112,该第一限位片112在膨胀状态下与第一缺口110的另一端抵接;也可只在第二缺口140的一端设置第二限位片142,该第二限位片142在膨胀状态下与第一缺口110的另一端抵接。Further, both ends of the first notch 110 are provided with a first limiting piece 112, corresponding to the extrusion interval left between the two first limiting pieces 112, both ends of the second notch 140 are provided with There are second limiting pieces 142 , and there is an extrusion space between the two second limiting pieces 142 . In the expanded state, since the expandable tube 10 is compressed and deformed, the corresponding two first limiting pieces 112 and the corresponding two second limiting pieces 142 gradually move closer until they abut against each other. At this time, the expandable tube 10 can no longer be squeezed out of shape. Optionally, the first limiting piece 112 can also be provided only at one end of the first notch 110, and the first limiting piece 112 abuts against the other end of the first notch 110 in the expanded state; One end of the notch 140 is provided with a second limiting piece 142 , and the second limiting piece 142 abuts against the other end of the first notch 110 in an expanded state.
进一步地,所述的椎体融合器还包括内芯20,所述内芯20设置在所述可膨胀管10内,且所述可膨胀管10的顶端与所述内芯20的顶端连接,所述内芯20的底端设有与变形工具匹配的螺纹。所述内芯20的顶端设有连扳210,所述内芯20的底端设有螺纹孔(图中未示出),所述膨胀管的顶端焊接在所述连扳210上,二者形成固定连接,所述螺纹孔与变形工具螺纹配合,变形时,所述变形工具的中芯拉住内芯20及可膨胀管10的顶端,然后所述变形工具能对可膨胀管10的底端进行挤压,使可膨胀管10两端相向受力,从而膨胀变形,膨胀过程是由可膨胀管10的顶端开始,逐渐发生变形。设置所述内芯20,一方面便于与变形工具配合连接,另一方面,提高整个椎体融合器的强度,而且使可膨胀管10的内部被填充,避免其向内变形凸起。根据实际需求,可直接在可膨胀管10的内壁上设置螺纹与变形工具配合,满足挤压需求。Further, the vertebral body fusion device further includes an inner core 20, the inner core 20 is arranged in the expandable tube 10, and the top end of the expandable tube 10 is connected to the top end of the inner core 20, The bottom end of the inner core 20 is provided with threads matched with the deformation tool. The top of the inner core 20 is provided with a connecting lever 210, the bottom of the inner core 20 is provided with a threaded hole (not shown in the figure), and the top of the expansion tube is welded on the connecting lever 210, both To form a fixed connection, the threaded hole is threadedly matched with the deforming tool. When deforming, the center core of the deforming tool pulls the inner core 20 and the top of the expandable tube 10, and then the deforming tool can touch the bottom of the expandable tube 10. Squeeze the ends of the expandable tube 10 so that the two ends of the expandable tube 10 are forced against each other, thereby expanding and deforming. The expansion process starts from the top of the expandable tube 10 and gradually deforms. The inner core 20 is set, on the one hand, it is convenient to be connected with the deformation tool, on the other hand, it improves the strength of the entire vertebral body cage, and makes the inside of the expandable tube 10 filled to avoid its inward deformation and protrusion. According to actual needs, threads can be directly provided on the inner wall of the expandable tube 10 to cooperate with the deformation tool to meet extrusion demands.
具体地,所述可膨胀管10的长度大于所述内芯20的长度,膨胀状态时,所述可膨胀管10的长度与所述内管或略长于内芯20。如此,使用时,椎体融合器结构更紧凑,使用更方便,同时便于变形工具与可膨胀管10底端对位进行挤压。Specifically, the length of the expandable tube 10 is greater than the length of the inner core 20 , and in the expanded state, the length of the expandable tube 10 is the same as the inner tube or slightly longer than the inner core 20 . In this way, when in use, the vertebral fusion cage has a more compact structure and is more convenient to use. At the same time, it is convenient for the deforming tool to align with the bottom end of the expandable tube 10 for extrusion.
进一步,所述椎体融合器的材质采用SUS304、PEEK、钛合金或者骨小梁金属等符合植入医疗器械标准的材质,表面处理方式可以为抛光、磨砂、等离子喷涂、喷涂纳米涂层等方式。本实施例所述可膨胀管10及内芯20为圆柱体,根据需求,也可以是长方体或者正方体。Further, the material of the vertebral body fusion device is made of SUS304, PEEK, titanium alloy or trabecular bone metal and other materials that meet the standards for implanting medical devices, and the surface treatment methods can be polishing, frosting, plasma spraying, spraying nano-coating, etc. . The expandable tube 10 and the inner core 20 in this embodiment are cylinders, and may also be cuboids or cubes according to requirements.
在其中一个实施例中,如图1-5所示,所述第二缺口140开设在所述可膨胀管10两端,即所述抗旋部150设置在所述可膨胀管10两端,在可膨胀管10靠近顶端及底端的位置设置抗旋部150,形成两个十字状结构,起到避免椎体融合器旋转的作用。在另一个实施中,如图6-9所示,在轴向方向上,所述第二缺口140与第一缺口110交替设置,即所述抗旋部150与撑起部120交替设置,设置一个由四个抗旋部150形成的十字状结构后,再设置一个由两个撑起部120形成的一字状结构,然后再设置十字结构,再设置一字结构,以此类推。十字状结构与一字结构的数量及排列顺序可根据需要设置。In one embodiment, as shown in FIGS. 1-5 , the second notch 140 is opened at both ends of the expandable tube 10 , that is, the anti-rotation portion 150 is provided at both ends of the expandable tube 10 , An anti-rotation part 150 is provided near the top end and the bottom end of the expandable tube 10 to form two cross-shaped structures to prevent rotation of the vertebral fusion cage. In another implementation, as shown in FIGS. 6-9 , in the axial direction, the second notches 140 are arranged alternately with the first notches 110 , that is, the anti-rotation parts 150 and the propping parts 120 are arranged alternately. After a cross-shaped structure formed by four anti-rotation parts 150, a straight-shaped structure formed by two propping parts 120 is arranged, and then a cross-shaped structure is arranged, and a straight-shaped structure is arranged again, and so on. The number and arrangement order of the cross-shaped structure and the one-word structure can be set as required.
以上所述实施例的各技术特征可以进行任意的组合,为使描述简洁,未对上述实施例中的各个技术特征所有可能的组合都进行描述,然而,只要这些技术特征的组合不存在矛盾,都应当认为是本说明书记载的范围。The technical features of the above-mentioned embodiments can be combined arbitrarily. To make the description concise, all possible combinations of the technical features in the above-mentioned embodiments are not described. However, as long as there is no contradiction in the combination of these technical features, should be considered as within the scope of this specification.
以上所述实施例仅表达了本发明的几种实施方式,其描述较为具体和详细,但并不能因此而理解为对发明专利范围的限制。应当指出的是,对于本领域的普通技术人员来说,在不脱离本发明构思的前提下,还可以做出若干变形和改进,这些都属于本发明的保护范围。因此,本发明专利的保护范围应以所附权利要求为准。The above-mentioned embodiments only express several implementation modes of the present invention, and the descriptions thereof are relatively specific and detailed, but should not be construed as limiting the patent scope of the invention. It should be pointed out that those skilled in the art can make several modifications and improvements without departing from the concept of the present invention, and these all belong to the protection scope of the present invention. Therefore, the protection scope of the patent for the present invention should be based on the appended claims.
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