US20160213380A1 - Occlusion device having spherical secondary shape and mandrel for forming same - Google Patents
Occlusion device having spherical secondary shape and mandrel for forming same Download PDFInfo
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- US20160213380A1 US20160213380A1 US15/003,308 US201615003308A US2016213380A1 US 20160213380 A1 US20160213380 A1 US 20160213380A1 US 201615003308 A US201615003308 A US 201615003308A US 2016213380 A1 US2016213380 A1 US 2016213380A1
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods
- A61B17/12—Surgical instruments, devices or methods for ligaturing or otherwise compressing tubular parts of the body, e.g. blood vessels or umbilical cord
- A61B17/12022—Occluding by internal devices, e.g. balloons or releasable wires
- A61B17/12131—Occluding by internal devices, e.g. balloons or releasable wires characterised by the type of occluding device
- A61B17/1214—Coils or wires
- A61B17/12145—Coils or wires having a pre-set deployed three-dimensional shape
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods
- A61B17/12—Surgical instruments, devices or methods for ligaturing or otherwise compressing tubular parts of the body, e.g. blood vessels or umbilical cord
- A61B17/12022—Occluding by internal devices, e.g. balloons or releasable wires
- A61B17/12099—Occluding by internal devices, e.g. balloons or releasable wires characterised by the location of the occluder
- A61B17/12109—Occluding by internal devices, e.g. balloons or releasable wires characterised by the location of the occluder in a blood vessel
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods
- A61B17/12—Surgical instruments, devices or methods for ligaturing or otherwise compressing tubular parts of the body, e.g. blood vessels or umbilical cord
- A61B17/12022—Occluding by internal devices, e.g. balloons or releasable wires
- A61B17/12099—Occluding by internal devices, e.g. balloons or releasable wires characterised by the location of the occluder
- A61B17/12109—Occluding by internal devices, e.g. balloons or releasable wires characterised by the location of the occluder in a blood vessel
- A61B17/12113—Occluding by internal devices, e.g. balloons or releasable wires characterised by the location of the occluder in a blood vessel within an aneurysm
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods
- A61B2017/00526—Methods of manufacturing
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods
- A61B2017/00743—Type of operation; Specification of treatment sites
- A61B2017/00778—Operations on blood vessels
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods
- A61B2017/00831—Material properties
- A61B2017/00867—Material properties shape memory effect
Definitions
- This application relates generally to occlusive devices for creating vascular occlusions.
- Vaso-occlusive devices are implants that are placed within the vasculature of the body to form occlusions in the vasculature, typically either to block the flow of blood through a vessel making up that portion of the vasculature via the formation of an embolus or to form an embolus within an aneurysm or other structure stemming from the vessel.
- the devices are typically implanted using a delivery catheter that is advanced endoluminally to the treatment site.
- vaso-occlusive device has an elongated helically-wound device having “primary shape” when constrained within a delivery catheter, and a three-dimensional “secondary” shape once deployed from the catheter and left, more or less, unconstrained in the implantation site. Because of the helical primary shape, these devices are generally referred to as vaso-occlusive coils.
- the coils are typically made of a relatively soft and flexible metal, for example, a platinum alloy, among others.
- one or more vaso-occlusive coils may be implanted.
- spherical devices that have a memorized spherical shape and comprise a wire having a memorized shape comprising a spherical outer wire layer and a spherical inner wire layer disposed within the spherical outer wire layer.
- the wire may be, for example, in the form of a coil with a helically wound primary shape (also referred to herein as a “helical coil”), and the memorized shape may comprise, for example, a spherical outer coil layer and a spherical inner coil layer disposed within the spherical outer coil layer.
- the inner coil layer may have a first shape that comprises multiple turns of a first spherical helix having a first axis and the outer coil layer may have a second shape that comprises multiple turns of a second spherical helix having a second axis.
- the inner coil layer may have a first shape that comprises 2 to 5 turns of a first spherical helix having a first axis and the outer coil layer may have a second shape that comprises 2 to 5 turns of a second spherical helix having a second axis.
- the first and second axes intersect at an angle ranging from 45° to 90°, typically ranging from 60° to a 90°, more typically ranging from 75° to 90°, even more typically ranging from 85° to 90°.
- the occlusion device may comprise an atraumatic distal coil tip.
- the inner coil layer and the outer coil layer of the occlusion device each comprises ends that do not protrude outside the spherical shape.
- the spherical mandrels comprise a first groove encircling the mandrel for multiple turns and a second groove encircling the mandrel for multiple turns, wherein the first and second grooves intersect and wherein the second groove is shallower than the first groove.
- the first groove may have a depth ranging from 1.5-2.0 D 1 while the second groove may have a depth ranging from 0.5-1.0 D 1 , where D 1 is the diameter of the wire (which may be in the form of a helical coil as previously noted).
- the first groove may have a first shape that comprises multiple turns of a first spherical helix having a first axis
- the second groove may have a second shape that comprises multiple turns of a second spherical helix having a second axis.
- the first and second axes intersect at an angle ranging from 45° to 90°, typically ranging from 60° to a 90°, more typically ranging from 75° to 90°, even more typically ranging from 85° to 90°.
- the mandrel may comprise a first anchor adjacent to the first groove and a second anchor adjacent the second groove.
- the spherical mandrels further comprise a directional member that is configured to permit a wire disposed on the mandrel to transition from the first groove to the second groove.
- Some aspects of the present disclosure pertain to methods of making an occlusion device that comprise (a) winding a wire onto a spherical mandrel like that described in any of the above aspects and embodiments, such that the wire is disposed within the first and second grooves; and (b) annealing the wire to form an occlusion device having a memorized shape (e.g., by applying heat for a time and temperature sufficient to form the memorized shape) comprising a spherical outer wire layer and a spherical inner wire layer disposed within the outer wire layer.
- a memorized shape e.g., by applying heat for a time and temperature sufficient to form the memorized shape
- the wire is onto the spherical mandrel by a process that comprises fixing a first end of the wire to a first anchor, winding the wire around the spherical mandrel using the first groove as a guide, changing a direction of a wind of the wire by engagement with a direction changing member, winding the wire around the spherical mandrel using the second groove as a guide, and attaching a second end of the wire to a second anchor.
- the wire may be in a form of a helical coil.
- Some aspects of the present disclosure pertain to methods of forming an occlusion comprising (a) advancing a catheter to an entrance of an aneurysm, (b) delivering an occlusion device comprising a wire through the catheter into the aneurysm, wherein the wire is constrained to a substantially linear shape when in the catheter and wherein, upon relaxation after delivery, the wire relaxes to a memorized spherical shape that comprises an outer wire layer and an inner wire layer disposed within the outer wire layer.
- the wire may be in a form of a helical coil that forms a spherical outer coil layer and a spherical inner coil layer disposed within the spherical outer coil layer.
- the inner coil layer may have a first shape that comprises multiple turns of a first spherical helix having a first axis and the outer coil layer may have a second shape that comprises multiple turns of a second spherical helix having a second axis.
- the inner coil layer may have a first shape that comprises 2 to 5 turns of a first spherical helix having a first axis and the inner coil layer may have a second shape that comprises 2 to 5 turns of a second spherical helix having a second axis.
- the first and second axes intersect at an angle ranging from 45° to 90°, typically ranging from 60° to a 90°, more typically ranging from 75° to 90°, even more typically ranging from 85° to 90°.
- FIG. 1 is a schematic illustration of a wire material having a primary coil shape
- FIGS. 2A-2D are schematic illustrations showing from various vantage points a secondary mandrel for forming an occlusion device
- FIG. 3 is a schematic illustration of a spherical helix having an axis A 1 ;
- FIG. 4 is a schematic illustration of an occlusion coil having a spherical secondary shape.
- the present disclosure pertains to spherical occlusion devices that comprise a wire having a memorized shape comprising (a) a spherical outer wire layer and (b) a spherical inner wire layer disposed within the spherical outer wire layer.
- the wire is in the form of a helical coil (i.e., a coil with a helically wound primary shape, for example, like that shown in FIG. 1 discussed below) that forms a spherical outer coil layer and a spherical inner coil layer disposed within the spherical outer coil layer, in which case the occlusion device may be referred to as an occlusion coil.
- Such an occlusion coil may be used, for example, as a framing coil when placed into the vasculature, for example, when placed in a vascular malformation such as an aneurysm or an arteriovenous malformation, among other uses.
- a “wire layer” and a “coil layer”, as used herein, are not solid layers but rather describe an overall shape that is formed by the wire (which wire may be in the form of a helical coil, in some embodiments).
- the occlusion device shown comprises a spherical inner coil layer formed by one end of a helical coil in the form of a first spherical helix and a spherical outer coil layer formed the other end of the helical coil in the form of a second spherical helix, which lies just outside the spherical inner coil layer in the form of the first spherical helix.
- spherical objects include those taking on a generally spheroidal shape, including those having the form of a perfect or near-perfect (to the eye) sphere and those having the form of a spheroid, such as a prolate spheroid (a slightly elongated sphere) or an oblate spheroid (a slightly flattened sphere), among other regular and irregular near-spherical geometries.
- a maximum diameter of the spherical secondary shape is between 1 and 1.5 times a minimum diameter of the spherical secondary shape, preferably between 1 and 1.2 times a minimum diameter of the spherical secondary shape, more preferably between 1 and 1.1 times a minimum diameter of the spherical secondary shape.
- a wire is typically wound around a small diameter, cylindrical primary mandrel to form a primary coil with a helical shape (also referred to herein as a primary shape coil or simply a coil) having a primary axis.
- the primary shape coil is then wound around a larger diameter secondary mandrel.
- the secondary mandrel and wound primary shape coil are then heated to a temperature and for a time sufficient to set or program the coil in a three-dimensional secondary shape.
- the secondary mandrel has a spherical shape and a wire that is wound around the mandrel and heat treated takes on a spherical secondary shape.
- Shape memory allows the wire, in its resting position, to assume the shape taken on by the wire when it was heat treated on the secondary mandrel.
- the wire is in the form of a coil. However, it is to be understood that the wire may be non-coiled as well.
- Suitable metals and alloys for forming the wire may include platinum group metals, particularly platinum, rhodium, palladium, and rhenium, as well as tungsten, gold, silver, tantalum, and alloys of these metals including platinum/tungsten alloy. These materials have significant radiopacity, and their alloys may be tailored to have a blend of flexibility and stiffness for the coil. They are also generally biologically inert.
- the wire may be constructed from, or otherwise include polymer fibers to promote blood clotting in the vessel.
- a wire 100 may be treated to assume a primary shape coil 110 that defines a primary axis 120 .
- the primary shape coil 110 has a primary diameter D 1 and can be formed using known manufacturing methods.
- the diameter of the primary shape coil may range, for example, from 0.012′′ to 0.021′′ (0.30 mm to 0.53 mm), among other values.
- the primary shape coil 110 may typically have about ten (e.g., 5 to 15) turns per centimeter, among other possibilities.
- the diameter of the wire may be between about 0.002′′ and 0.005′′ (0.05 mm and 0.13 mm), among other values.
- Such a wire 100 may be of an appropriate diameter, for example, to provide sufficient radial force to hold the occlusion device in place within a chosen body cavity without distending the wall of the cavity and/or without moving substantially from the cavity as a result of the repetitive fluid pulsing experienced within the vascular system.
- the wire 100 having the primary shape 110 may be treated further to assume a secondary shape as discussed below.
- the wire may be wound around a secondary mandrel.
- the secondary mandrel and the wound wire are then heat treated to program or set the wire in an appropriate memorized secondary shape.
- Secondary mandrels in accordance with the present disclosure are spherical in shape.
- a specific example of such a secondary mandrel 200 is shown in FIGS. 2A-2D .
- the diameter D 2 of the secondary mandrel 200 will correspond approximately to the desired secondary coil shape diameter.
- the anchors 210 f , 210 s may be designed such that they do not protrude outside the spherical shape, for example by providing a hole with set screw or other fixation means.
- Occlusion devices such as occlusion coils commonly have an atraumatic tip on one end of the coil.
- the starting anchoring point 210 f may be designed to hold the atraumatic end of a coil in some embodiments. Forming an atruamatic end prior to the secondary winding process may prevent more costly defects associated with the formation of an atruamatic tip at a later stage in the process.
- there is also a directional member 215 which allows a winding direction of the wire to the changed during the winding process.
- the directional member 215 may be, for example, in the form of a loop or peg or other suitable structure.
- the mandrel 200 comprises a first groove 220 f in the form of a first spherical helix having a first axis A 1 . Because a single spherical helix 300 is substantially mechanically compressible along its axis A 1 (see FIG. 3 ), a second groove 220 s in the form of a second spherical helix having a second axis A 2 is provided, and the axes A 1 , A 2 of the first and second helices are rotated relative to one another by predetermined angle.
- the first and second axes A 1 , A 2 cross one another at an angle ranging from 45° or less up to 90° (the maximum possible value), for example ranging from 45° to 50° to 55° to 60° to 65° to 70° to 75° to 80° to 85° to 87.5° to 90° (i.e., ranging between any two of the preceding values), typically crossing one another at an angle ranging from 60° to a 90°, more typically ranging from 75° to 90°, even more typically ranging from 85° to 90°.
- the mandrel 200 is designed such that an inner layer of wire that is wound on the mandrel 200 using first groove 220 f as a guide will be positioned below the outer layer of wire that is wound on the mandrel 200 using second groove 220 s as a guide. Consequently, the first groove 220 f may be provided with a depth that is deeper than that of the second groove 220 s , for example, in some embodiments, deeper by a depth corresponding to the diameter of the wire to be wound (e.g., D 1 in the case of a primary shape coil). As one example, the first groove may have a depth of 1.5 D 1 whereas the second groove may have a depth of 0.5 D 1 .
- the first groove may have a depth of 2.0 D 1 whereas the second groove may have a depth of 1.0 D 1 .
- the width w of the first groove 220 f will typically be at least D 1 , beneficially, about 1.5 D 1 .
- the width of the second groove may be less than D 1 in some embodiments, as the wire being wound need not fit entirely within the second groove 220 s .
- the mandrel may be provided with a handle 230 (a portion of which is shown in FIGS. 2A, 2C and 2D ) to allow an operator to maneuver the coil and mandrel.
- Secondary mandrels in accordance with the present disclosure may be formed from a variety of known materials capable of being heated during device manufacturing, e.g., when the wire is heat treated.
- Exemplary secondary mandrel materials may include metals such as stainless steel, as well as ceramic or other refractory materials including, but not limited to, alumina or zirconia.
- the secondary mandrel may be made from stainless steel and may be manufactured using 3D laser printing. As previously indicated, the secondary mandrel provides a support for winding a wire and provides a specific secondary shape when the secondary mandrel and wire are heated.
- the wire Prior to heat treatment, the wire may be wound around the mandrel in a sequence to give the coil a spherical secondary shape.
- a wire may be (a) affixed at the first anchor 210 f , (b) wound around the mandrel 200 in a first direction using the spherical helical first groove 220 f as a guide, (c) placed into engagement with the directional member 215 (i.e., threaded through a loop associated with the directional member 215 in the embodiment shown), allowing a winding direction of the wire to be changed such that the wire can be (d) wound around the mandrel 200 in a second direction using the spherical helical second groove 220 s as a guide, and (e) secured to the second anchor 210 s .
- the diameter D 2 of the secondary mandrel (after taking into account groove depth) will correspond to the required outer diameter of the resulting occlusion device.
- the wire is then heat treated to retain the secondary structure.
- a wire made of a platinum, palladium, or platinum/tungsten alloy, among other possibilities may be wound around the secondary mandrel and can be heated to a suitable temperature for a suitable time to program or set the secondary shape.
- Heating temperatures and durations can vary with different materials. In one specific example where nitinol is selected as a material, the temperature may range, for instance, from 460° C. to 530° C. and the time may vary, for instance, from 1 to 30 minutes, among other possibilities.
- the occlusion device may be removed from the mandrel.
- an inner wire layer e.g., an inner coil layer
- an outer wire layer e.g., an outer coil layer
- axes of the two spherical helices cross one another at an angle dictated by the grooves of the mandrel, for example, crossing one another at an angle ranging from 45° or less to 90° (the maximum possible value), for example ranging from 45° to 50° to 55° to 60° to 65° to 70° to 75° to 80° to 85° to 87.5° to 90°, typically crossing one another at an angle ranging from 60° to a 90°, more typically ranging from 75° to 90°, even more typically ranging from 85° to 90°.
- an annealed spherical occlusion device with a secondary structure comprising two coil layers may be produced, in which an inner coil layer 110 i in the form of a first spherical helix having approximately five turns and having an axis A 1 is positioned below an outer coil layer 110 o in the form of a second spherical helix having approximately five turns and having an axis A 2 , which oriented at a 90° angle with respect to axis A 1 .
- Such an occlusion device differs somewhat from a device produced by the mandrel of FIGS. 2A-2D , for example, in that an inner coil layer produced by mandrel of FIGS. 2A-2D is in the form of a first spherical helix having approximately four turns and an outer coil layer produced by the mandrel of FIGS. 2A-2D is in the form of a second spherical helix having approximately three turns.
- occlusion devices in accordance with the present disclosure may be formed having a variety of diameters. Typical diameters range, for example, from about 6 mm to 20 mm, among other values. Typically, the inner and outer wire layers will have between 2 and 5 turns, among other values.
- the resulting occlusion device may be constrained in a primary (substantially linear) configuration and may be provided with a shape memory that biases the coil to assume a three-dimensional spherical secondary configuration when in a relaxed state.
- the coil when it is not restricted by external forces or barriers, it may assume a relaxed, three-dimensional secondary shape such as that shown in FIG. 4 , among many other possibilities.
- the occlusion device may assume a primary (substantially linear) configuration when it is disposed within a catheter or other delivery device used to deliver the coil into a patient's body.
- a catheter may be introduced into a patient's body, generally from a percutaneous entry site, e.g., into a peripheral artery, such as the femoral or carotid arteries (not shown), as is known in the art.
- the catheter may be advanced over a guidewire or other rail previously placed within the patient's vasculature using known methods.
- the catheter may be advanced through the patient's vasculature until a distal end of the catheter is disposed within a blood vessel adjacent to an aneurysm or other vascular malformation.
- an occlusion device may be advanced through a lumen of the catheter in a primary (substantially linear) configuration, emerging from a distal tip of the catheter and into the vascular malformation. As the occlusion device is deployed and allowed to relax, it assumes a three-dimensional secondary configuration, as previously discussed. In certain beneficial embodiments, the secondary configuration is selected so that the occlusion device substantially fills the vascular malformation.
- the occlusion device may be delivered using delivery wire which can be connected using an interlocking detachment system as is known in the art. Advancing the delivery wire will deploy the occlusion device out of the catheter. The catheter may be removed after the occlusion device is fully deployed within the aneurysm, as is known in the art.
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Abstract
Description
- This application claims the benefit of U.S. Provisional Application No. 62/106,445, filed Jan. 22, 2015, entitled “OCCLUSION DEVICE HAVING SPHERICAL SECONDARY SHAPE AND MANDREL FOR FORMING SAME,” which is hereby incorporated by reference in its entirety.
- This application relates generally to occlusive devices for creating vascular occlusions.
- Vaso-occlusive devices are implants that are placed within the vasculature of the body to form occlusions in the vasculature, typically either to block the flow of blood through a vessel making up that portion of the vasculature via the formation of an embolus or to form an embolus within an aneurysm or other structure stemming from the vessel. The devices are typically implanted using a delivery catheter that is advanced endoluminally to the treatment site.
- An example of a well-known vaso-occlusive device has an elongated helically-wound device having “primary shape” when constrained within a delivery catheter, and a three-dimensional “secondary” shape once deployed from the catheter and left, more or less, unconstrained in the implantation site. Because of the helical primary shape, these devices are generally referred to as vaso-occlusive coils. The coils are typically made of a relatively soft and flexible metal, for example, a platinum alloy, among others. Depending on the size and/or shape of the implantation space, one or more vaso-occlusive coils may be implanted.
- Some aspects of the present disclosure pertain to spherical devices that have a memorized spherical shape and comprise a wire having a memorized shape comprising a spherical outer wire layer and a spherical inner wire layer disposed within the spherical outer wire layer. The wire may be, for example, in the form of a coil with a helically wound primary shape (also referred to herein as a “helical coil”), and the memorized shape may comprise, for example, a spherical outer coil layer and a spherical inner coil layer disposed within the spherical outer coil layer.
- In various embodiments, which may be used in combination with any of the above aspects and embodiments, the inner coil layer may have a first shape that comprises multiple turns of a first spherical helix having a first axis and the outer coil layer may have a second shape that comprises multiple turns of a second spherical helix having a second axis.
- In various embodiments, which may be used in combination with any of the above aspects and embodiments, the inner coil layer may have a first shape that comprises 2 to 5 turns of a first spherical helix having a first axis and the outer coil layer may have a second shape that comprises 2 to 5 turns of a second spherical helix having a second axis.
- In various embodiments, which may be used in combination with any of the above aspects and embodiments, the first and second axes intersect at an angle ranging from 45° to 90°, typically ranging from 60° to a 90°, more typically ranging from 75° to 90°, even more typically ranging from 85° to 90°.
- In various embodiments, which may be used in combination with any of the above aspects and embodiments, the occlusion device may comprise an atraumatic distal coil tip.
- In various embodiments, which may be used in combination with any of the above aspects and embodiments, the inner coil layer and the outer coil layer of the occlusion device each comprises ends that do not protrude outside the spherical shape.
- Some aspects of the present disclosure pertain to spherical mandrels for producing a spherical occlusion device. The spherical mandrels comprise a first groove encircling the mandrel for multiple turns and a second groove encircling the mandrel for multiple turns, wherein the first and second grooves intersect and wherein the second groove is shallower than the first groove. For example, in certain embodiments, the first groove may have a depth ranging from 1.5-2.0 D1 while the second groove may have a depth ranging from 0.5-1.0 D1, where D1 is the diameter of the wire (which may be in the form of a helical coil as previously noted).
- In various embodiments, which may be used in combination with any of the above aspects and embodiments, the first groove may have a first shape that comprises multiple turns of a first spherical helix having a first axis, and the second groove may have a second shape that comprises multiple turns of a second spherical helix having a second axis.
- In various embodiments, which may be used in combination with any of the above aspects and embodiments, the first and second axes intersect at an angle ranging from 45° to 90°, typically ranging from 60° to a 90°, more typically ranging from 75° to 90°, even more typically ranging from 85° to 90°.
- In various embodiments, which may be used in combination with any of the above aspects and embodiments, the mandrel may comprise a first anchor adjacent to the first groove and a second anchor adjacent the second groove.
- In various embodiments, which may be used in combination with any of the above aspects and embodiments, the spherical mandrels further comprise a directional member that is configured to permit a wire disposed on the mandrel to transition from the first groove to the second groove.
- Some aspects of the present disclosure pertain to methods of making an occlusion device that comprise (a) winding a wire onto a spherical mandrel like that described in any of the above aspects and embodiments, such that the wire is disposed within the first and second grooves; and (b) annealing the wire to form an occlusion device having a memorized shape (e.g., by applying heat for a time and temperature sufficient to form the memorized shape) comprising a spherical outer wire layer and a spherical inner wire layer disposed within the outer wire layer.
- In some embodiments, the wire is onto the spherical mandrel by a process that comprises fixing a first end of the wire to a first anchor, winding the wire around the spherical mandrel using the first groove as a guide, changing a direction of a wind of the wire by engagement with a direction changing member, winding the wire around the spherical mandrel using the second groove as a guide, and attaching a second end of the wire to a second anchor.
- In various embodiments, which may be used in combination with any of the above aspects and embodiments, the wire may be in a form of a helical coil.
- Some aspects of the present disclosure pertain to methods of forming an occlusion comprising (a) advancing a catheter to an entrance of an aneurysm, (b) delivering an occlusion device comprising a wire through the catheter into the aneurysm, wherein the wire is constrained to a substantially linear shape when in the catheter and wherein, upon relaxation after delivery, the wire relaxes to a memorized spherical shape that comprises an outer wire layer and an inner wire layer disposed within the outer wire layer.
- In various embodiments, which may be used in combination with any of the above aspects and embodiments, the wire may be in a form of a helical coil that forms a spherical outer coil layer and a spherical inner coil layer disposed within the spherical outer coil layer.
- In various embodiments, which may be used in combination with any of the above aspects and embodiments, the inner coil layer may have a first shape that comprises multiple turns of a first spherical helix having a first axis and the outer coil layer may have a second shape that comprises multiple turns of a second spherical helix having a second axis.
- In various embodiments, which may be used in combination with any of the above aspects and embodiments, the inner coil layer may have a first shape that comprises 2 to 5 turns of a first spherical helix having a first axis and the inner coil layer may have a second shape that comprises 2 to 5 turns of a second spherical helix having a second axis.
- In various embodiments, which may be used in combination with any of the above aspects and embodiments, the first and second axes intersect at an angle ranging from 45° to 90°, typically ranging from 60° to a 90°, more typically ranging from 75° to 90°, even more typically ranging from 85° to 90°.
- These and other aspects, embodiments and advantages of the present invention will become immediately apparent to those of ordinary skill in the art upon review of the detailed description and claims to follow.
- Aspects of the present disclosure are described below with reference to the following drawings in which like numerals reference like elements, and wherein:
-
FIG. 1 is a schematic illustration of a wire material having a primary coil shape; -
FIGS. 2A-2D are schematic illustrations showing from various vantage points a secondary mandrel for forming an occlusion device; -
FIG. 3 is a schematic illustration of a spherical helix having an axis A1; and -
FIG. 4 is a schematic illustration of an occlusion coil having a spherical secondary shape. - Unless otherwise provided in the following specification, the drawings are not necessarily to scale, with emphasis being placed on illustration of the principles of the invention.
- According to one aspect, the present disclosure pertains to spherical occlusion devices that comprise a wire having a memorized shape comprising (a) a spherical outer wire layer and (b) a spherical inner wire layer disposed within the spherical outer wire layer. In certain beneficial embodiments, the wire is in the form of a helical coil (i.e., a coil with a helically wound primary shape, for example, like that shown in
FIG. 1 discussed below) that forms a spherical outer coil layer and a spherical inner coil layer disposed within the spherical outer coil layer, in which case the occlusion device may be referred to as an occlusion coil. Such an occlusion coil may be used, for example, as a framing coil when placed into the vasculature, for example, when placed in a vascular malformation such as an aneurysm or an arteriovenous malformation, among other uses. - It is to be understood that a “wire layer” and a “coil layer”, as used herein, are not solid layers but rather describe an overall shape that is formed by the wire (which wire may be in the form of a helical coil, in some embodiments). For example, in
FIG. 4 , discussed in detail below, the occlusion device shown comprises a spherical inner coil layer formed by one end of a helical coil in the form of a first spherical helix and a spherical outer coil layer formed the other end of the helical coil in the form of a second spherical helix, which lies just outside the spherical inner coil layer in the form of the first spherical helix. - As used herein spherical objects include those taking on a generally spheroidal shape, including those having the form of a perfect or near-perfect (to the eye) sphere and those having the form of a spheroid, such as a prolate spheroid (a slightly elongated sphere) or an oblate spheroid (a slightly flattened sphere), among other regular and irregular near-spherical geometries. In certain embodiments, a maximum diameter of the spherical secondary shape is between 1 and 1.5 times a minimum diameter of the spherical secondary shape, preferably between 1 and 1.2 times a minimum diameter of the spherical secondary shape, more preferably between 1 and 1.1 times a minimum diameter of the spherical secondary shape.
- During the process of manufacturing an occlusion coil, a wire is typically wound around a small diameter, cylindrical primary mandrel to form a primary coil with a helical shape (also referred to herein as a primary shape coil or simply a coil) having a primary axis. The primary shape coil is then wound around a larger diameter secondary mandrel. The secondary mandrel and wound primary shape coil are then heated to a temperature and for a time sufficient to set or program the coil in a three-dimensional secondary shape.
- In the present disclosure, the secondary mandrel has a spherical shape and a wire that is wound around the mandrel and heat treated takes on a spherical secondary shape. Shape memory allows the wire, in its resting position, to assume the shape taken on by the wire when it was heat treated on the secondary mandrel. In various embodiments described herein, the wire is in the form of a coil. However, it is to be understood that the wire may be non-coiled as well.
- Suitable metals and alloys for forming the wire may include platinum group metals, particularly platinum, rhodium, palladium, and rhenium, as well as tungsten, gold, silver, tantalum, and alloys of these metals including platinum/tungsten alloy. These materials have significant radiopacity, and their alloys may be tailored to have a blend of flexibility and stiffness for the coil. They are also generally biologically inert.
- Alternatively or in addition, the wire may be constructed from, or otherwise include polymer fibers to promote blood clotting in the vessel.
- Referring now to
FIG. 1 , in some embodiments, awire 100 may be treated to assume aprimary shape coil 110 that defines aprimary axis 120. Theprimary shape coil 110 has a primary diameter D1 and can be formed using known manufacturing methods. The diameter of the primary shape coil may range, for example, from 0.012″ to 0.021″ (0.30 mm to 0.53 mm), among other values. Theprimary shape coil 110 may typically have about ten (e.g., 5 to 15) turns per centimeter, among other possibilities. When thewire 100 is made from a metal or metal alloy, the diameter of the wire may be between about 0.002″ and 0.005″ (0.05 mm and 0.13 mm), among other values. Such awire 100 may be of an appropriate diameter, for example, to provide sufficient radial force to hold the occlusion device in place within a chosen body cavity without distending the wall of the cavity and/or without moving substantially from the cavity as a result of the repetitive fluid pulsing experienced within the vascular system. - The
wire 100 having theprimary shape 110 may be treated further to assume a secondary shape as discussed below. In this regard, after the wire has been set it itsprimary shape 110, the wire may be wound around a secondary mandrel. The secondary mandrel and the wound wire are then heat treated to program or set the wire in an appropriate memorized secondary shape. - Secondary mandrels in accordance with the present disclosure are spherical in shape. A specific example of such a
secondary mandrel 200 is shown inFIGS. 2A-2D . Referring toFIG. 2A , the diameter D2 of thesecondary mandrel 200 will correspond approximately to the desired secondary coil shape diameter. In the embodiment shown, there are anchoring points at positions around thesecondary mandrel 200 to hold the wire (e.g., primary shape coil) in position, in particular, afirst anchor 210 f for the start of the winding process and asecond anchoring point 210 s for the completion of the winding process. Although not shown, the 210 f, 210 s may be designed such that they do not protrude outside the spherical shape, for example by providing a hole with set screw or other fixation means. Occlusion devices such as occlusion coils commonly have an atraumatic tip on one end of the coil. Theanchors starting anchoring point 210 f may be designed to hold the atraumatic end of a coil in some embodiments. Forming an atruamatic end prior to the secondary winding process may prevent more costly defects associated with the formation of an atruamatic tip at a later stage in the process. In the embodiment shown, there is also adirectional member 215 which allows a winding direction of the wire to the changed during the winding process. Thedirectional member 215 may be, for example, in the form of a loop or peg or other suitable structure. - In the design shown, the
mandrel 200 comprises afirst groove 220 f in the form of a first spherical helix having a first axis A1. Because a singlespherical helix 300 is substantially mechanically compressible along its axis A1 (seeFIG. 3 ), asecond groove 220 s in the form of a second spherical helix having a second axis A2 is provided, and the axes A1, A2 of the first and second helices are rotated relative to one another by predetermined angle. In certain beneficial embodiments, the first and second axes A1, A2 cross one another at an angle ranging from 45° or less up to 90° (the maximum possible value), for example ranging from 45° to 50° to 55° to 60° to 65° to 70° to 75° to 80° to 85° to 87.5° to 90° (i.e., ranging between any two of the preceding values), typically crossing one another at an angle ranging from 60° to a 90°, more typically ranging from 75° to 90°, even more typically ranging from 85° to 90°. In the embodiment shown, themandrel 200 is designed such that an inner layer of wire that is wound on themandrel 200 usingfirst groove 220 f as a guide will be positioned below the outer layer of wire that is wound on themandrel 200 usingsecond groove 220 s as a guide. Consequently, thefirst groove 220 f may be provided with a depth that is deeper than that of thesecond groove 220 s, for example, in some embodiments, deeper by a depth corresponding to the diameter of the wire to be wound (e.g., D1 in the case of a primary shape coil). As one example, the first groove may have a depth of 1.5 D1 whereas the second groove may have a depth of 0.5 D1. As another example, the first groove may have a depth of 2.0 D1 whereas the second groove may have a depth of 1.0 D1. The width w of thefirst groove 220 f will typically be at least D1, beneficially, about 1.5 D1. The width of the second groove may be less than D1 in some embodiments, as the wire being wound need not fit entirely within thesecond groove 220 s. The mandrel may be provided with a handle 230 (a portion of which is shown inFIGS. 2A, 2C and 2D ) to allow an operator to maneuver the coil and mandrel. - Secondary mandrels in accordance with the present disclosure may be formed from a variety of known materials capable of being heated during device manufacturing, e.g., when the wire is heat treated. Exemplary secondary mandrel materials may include metals such as stainless steel, as well as ceramic or other refractory materials including, but not limited to, alumina or zirconia. In one beneficial embodiment, the secondary mandrel may be made from stainless steel and may be manufactured using 3D laser printing. As previously indicated, the secondary mandrel provides a support for winding a wire and provides a specific secondary shape when the secondary mandrel and wire are heated.
- Prior to heat treatment, the wire may be wound around the mandrel in a sequence to give the coil a spherical secondary shape. For example, with reference to
FIGS. 2A-2D , a wire may be (a) affixed at thefirst anchor 210 f, (b) wound around themandrel 200 in a first direction using the spherical helicalfirst groove 220 f as a guide, (c) placed into engagement with the directional member 215 (i.e., threaded through a loop associated with thedirectional member 215 in the embodiment shown), allowing a winding direction of the wire to be changed such that the wire can be (d) wound around themandrel 200 in a second direction using the spherical helicalsecond groove 220 s as a guide, and (e) secured to thesecond anchor 210 s. The diameter D2 of the secondary mandrel (after taking into account groove depth) will correspond to the required outer diameter of the resulting occlusion device. The wire is then heat treated to retain the secondary structure. For example, a wire made of a platinum, palladium, or platinum/tungsten alloy, among other possibilities, may be wound around the secondary mandrel and can be heated to a suitable temperature for a suitable time to program or set the secondary shape. Persons of ordinary skill in the art will recognize that heating temperatures and durations can vary with different materials. In one specific example where nitinol is selected as a material, the temperature may range, for instance, from 460° C. to 530° C. and the time may vary, for instance, from 1 to 30 minutes, among other possibilities. After heat treatment, the occlusion device may be removed from the mandrel. - In this way a secondary structure with an inner wire layer and an outer wire layer may be produced, in which an inner wire layer (e.g., an inner coil layer) in the form of a first spherical helix sits below an outer wire layer (e.g., an outer coil layer) in the form of a second spherical helix. In various embodiments, axes of the two spherical helices cross one another at an angle dictated by the grooves of the mandrel, for example, crossing one another at an angle ranging from 45° or less to 90° (the maximum possible value), for example ranging from 45° to 50° to 55° to 60° to 65° to 70° to 75° to 80° to 85° to 87.5° to 90°, typically crossing one another at an angle ranging from 60° to a 90°, more typically ranging from 75° to 90°, even more typically ranging from 85° to 90°.
- As one specific example shown in
FIG. 4 , an annealed spherical occlusion device with a secondary structure comprising two coil layers may be produced, in which aninner coil layer 110 i in the form of a first spherical helix having approximately five turns and having an axis A1 is positioned below an outer coil layer 110 o in the form of a second spherical helix having approximately five turns and having an axis A2, which oriented at a 90° angle with respect to axis A1. - Such an occlusion device differs somewhat from a device produced by the mandrel of
FIGS. 2A-2D , for example, in that an inner coil layer produced by mandrel ofFIGS. 2A-2D is in the form of a first spherical helix having approximately four turns and an outer coil layer produced by the mandrel ofFIGS. 2A-2D is in the form of a second spherical helix having approximately three turns. - As can be seen from the preceding description, occlusion devices in accordance with the present disclosure may be formed having a variety of diameters. Typical diameters range, for example, from about 6 mm to 20 mm, among other values. Typically, the inner and outer wire layers will have between 2 and 5 turns, among other values.
- In use, the resulting occlusion device may be constrained in a primary (substantially linear) configuration and may be provided with a shape memory that biases the coil to assume a three-dimensional spherical secondary configuration when in a relaxed state. Thus, when the coil is not restricted by external forces or barriers, it may assume a relaxed, three-dimensional secondary shape such as that shown in
FIG. 4 , among many other possibilities. For example, the occlusion device may assume a primary (substantially linear) configuration when it is disposed within a catheter or other delivery device used to deliver the coil into a patient's body. - In one specific embodiment, a catheter may be introduced into a patient's body, generally from a percutaneous entry site, e.g., into a peripheral artery, such as the femoral or carotid arteries (not shown), as is known in the art. The catheter may be advanced over a guidewire or other rail previously placed within the patient's vasculature using known methods. For example, in one particular embodiment, the catheter may be advanced through the patient's vasculature until a distal end of the catheter is disposed within a blood vessel adjacent to an aneurysm or other vascular malformation. Once the catheter is properly positioned, an occlusion device may be advanced through a lumen of the catheter in a primary (substantially linear) configuration, emerging from a distal tip of the catheter and into the vascular malformation. As the occlusion device is deployed and allowed to relax, it assumes a three-dimensional secondary configuration, as previously discussed. In certain beneficial embodiments, the secondary configuration is selected so that the occlusion device substantially fills the vascular malformation. The occlusion device may be delivered using delivery wire which can be connected using an interlocking detachment system as is known in the art. Advancing the delivery wire will deploy the occlusion device out of the catheter. The catheter may be removed after the occlusion device is fully deployed within the aneurysm, as is known in the art.
- Although various embodiments are specifically illustrated and described herein, it will be appreciated that modifications and variations of the present disclosure are covered by the above teachings and are within the purview of the appended claims without departing from the spirit and intended scope of the invention.
Claims (20)
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US15/003,308 US20160213380A1 (en) | 2015-01-22 | 2016-01-21 | Occlusion device having spherical secondary shape and mandrel for forming same |
| US17/537,812 US12508033B2 (en) | 2015-01-22 | 2021-11-30 | Occlusion device having spherical secondary shape and mandrel for forming same |
Applications Claiming Priority (2)
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|---|---|---|---|
| US201562106445P | 2015-01-22 | 2015-01-22 | |
| US15/003,308 US20160213380A1 (en) | 2015-01-22 | 2016-01-21 | Occlusion device having spherical secondary shape and mandrel for forming same |
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| Application Number | Title | Priority Date | Filing Date |
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| US17/537,812 Continuation US12508033B2 (en) | 2015-01-22 | 2021-11-30 | Occlusion device having spherical secondary shape and mandrel for forming same |
Publications (1)
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| US20160213380A1 true US20160213380A1 (en) | 2016-07-28 |
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| US17/537,812 Active 2038-12-22 US12508033B2 (en) | 2015-01-22 | 2021-11-30 | Occlusion device having spherical secondary shape and mandrel for forming same |
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| US17/537,812 Active 2038-12-22 US12508033B2 (en) | 2015-01-22 | 2021-11-30 | Occlusion device having spherical secondary shape and mandrel for forming same |
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| CN113634564A (en) * | 2021-09-16 | 2021-11-12 | 深圳市博立生物材料有限公司 | A kind of degradable cleaning ball and its making method |
| US11191611B2 (en) | 2016-06-03 | 2021-12-07 | Somatex Medical Technologies Gmbh | Marking device and implantation system |
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| US11357511B2 (en) | 2008-05-01 | 2022-06-14 | Aneuclose Llc | Intrasacular aneurysm occlusion device with globular first configuration and bowl-shaped second configuration |
| US11406404B2 (en) | 2020-02-20 | 2022-08-09 | Cerus Endovascular Limited | Clot removal distal protection methods |
| US11464518B2 (en) | 2008-05-01 | 2022-10-11 | Aneuclose Llc | Proximal concave neck bridge with central lumen and distal net for occluding cerebral aneurysms |
| US11471164B2 (en) | 2008-05-01 | 2022-10-18 | Aneuclose Llc | Methods of occluding a cerebral aneurysm by inserting embolic members or material into an intrasacular implant |
| US11471163B2 (en) | 2008-05-01 | 2022-10-18 | Aneuclose Llc | Intrasaccular aneurysm occlusion device with net or mesh expanded by string-of-pearls embolies |
| US11471162B2 (en) | 2015-12-07 | 2022-10-18 | Cerus Endovascular Limited | Occlusion device |
| US11484322B2 (en) | 2018-01-03 | 2022-11-01 | Aneuclose Llc | Aneurysm neck bridge with a closeable opening or lumen through which embolic material is inserted into the aneurysm sac |
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| US11583289B2 (en) | 2008-05-01 | 2023-02-21 | Aneuclose Llc | Aneurysm-occluding mesh ribbon with a series of loops or segments having distal-to-proximal variation in size, shape, and/or orientation |
| US11357511B2 (en) | 2008-05-01 | 2022-06-14 | Aneuclose Llc | Intrasacular aneurysm occlusion device with globular first configuration and bowl-shaped second configuration |
| US11464518B2 (en) | 2008-05-01 | 2022-10-11 | Aneuclose Llc | Proximal concave neck bridge with central lumen and distal net for occluding cerebral aneurysms |
| US11471164B2 (en) | 2008-05-01 | 2022-10-18 | Aneuclose Llc | Methods of occluding a cerebral aneurysm by inserting embolic members or material into an intrasacular implant |
| US11471163B2 (en) | 2008-05-01 | 2022-10-18 | Aneuclose Llc | Intrasaccular aneurysm occlusion device with net or mesh expanded by string-of-pearls embolies |
| US12414775B1 (en) | 2014-04-30 | 2025-09-16 | Stryker Ireland Technology LTD | Occlusion device |
| US11284901B2 (en) | 2014-04-30 | 2022-03-29 | Cerus Endovascular Limited | Occlusion device |
| US11389174B2 (en) | 2014-04-30 | 2022-07-19 | Cerus Endovascular Limited | Occlusion device |
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| US12076022B2 (en) | 2015-12-07 | 2024-09-03 | Stryker Ireland Technology Ltd. | Occlusion device |
| US11471162B2 (en) | 2015-12-07 | 2022-10-18 | Cerus Endovascular Limited | Occlusion device |
| US12285175B2 (en) | 2016-03-11 | 2025-04-29 | Stryker Ireland Technology Ltd. | Occlusion device |
| US11648013B2 (en) | 2016-03-11 | 2023-05-16 | Cerus Endovascular Limited | Occlusion device |
| US11779432B2 (en) | 2016-06-03 | 2023-10-10 | Somatex Medical Technologies Gmbh | Marking device and implantation system |
| US12150822B2 (en) | 2016-06-03 | 2024-11-26 | Somatex Medical Technologies Gmbh | Marking device and implantation system |
| US11191611B2 (en) | 2016-06-03 | 2021-12-07 | Somatex Medical Technologies Gmbh | Marking device and implantation system |
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| US11812971B2 (en) | 2017-08-21 | 2023-11-14 | Cerus Endovascular Limited | Occlusion device |
| US12251112B2 (en) | 2017-08-21 | 2025-03-18 | Stryker Ireland Technology Ltd. | Occlusion device |
| US11484322B2 (en) | 2018-01-03 | 2022-11-01 | Aneuclose Llc | Aneurysm neck bridge with a closeable opening or lumen through which embolic material is inserted into the aneurysm sac |
| US12521202B2 (en) | 2019-11-29 | 2026-01-13 | Somatex Medical Technologies Gmbh | Marking element for marking tissue |
| US11406404B2 (en) | 2020-02-20 | 2022-08-09 | Cerus Endovascular Limited | Clot removal distal protection methods |
| US12303153B2 (en) | 2020-02-20 | 2025-05-20 | Stryker Ireland Technology Ltd. | Clot removal distal protection methods |
| CN113634564A (en) * | 2021-09-16 | 2021-11-12 | 深圳市博立生物材料有限公司 | A kind of degradable cleaning ball and its making method |
| CN116236236A (en) * | 2022-12-21 | 2023-06-09 | 南京思脉德医疗科技有限公司 | Oval hole blood sealing plug and plugging device |
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| US12508033B2 (en) | 2025-12-30 |
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