Abstract: The present invention relates in general to anchoring systems for occluder devices, and more specifically, to an anchoring system and method for implanting an occluder device within a left atrial appendage (“LAA”) of the heart. The anchoring system is configured so that an anchor penetrates the inner endocardium layer, middle myocardium layer, and outer epicardium layer of an LAA wall. The purpose of the present invention is to provide an occluder device anchor that has a low risk of embolization and/or causing injury to neighboring valve structures. An additional purpose of the present invention is to provide an anchoring system and method for implanting an occluder device within the LAA that allows for the occluder device to be retrievable after initial placement, reusable, and repositionable for an optimal final placement within the LAA.

Abstract: The present invention relates in general to anchoring systems for occluder devices, and more specifically, to an anchoring system and method for implanting an occluder device within a left atrial appendage (“LAA”) of the heart. The anchoring system is configured so that an anchor penetrates the inner endocardium layer, middle myocardium layer, and outer epicardium layer of an LAA wall. The purpose of the present invention is to provide an occluder device anchor that has a low risk of embolization and/or causing injury to neighboring valve structures. An additional purpose of the present invention is to provide an anchoring system and method for implanting an occluder device within the LAA that allows for the occluder device to be retrievable after initial placement, reusable, and repositionable for an optimal final placement within the LAA.

Abstract: This disclosure is directed to an aperture occlusion device and a method for occluding an aperture, including a perimembranous ventricular septal defect. The aperture occlusion device includes a wire frame element. The wire frame forms geometric shapes that include an occluder region and a securing region. The occluder region and the securing region are separated by an attachment region including a waist. The occluder region and securing region can include membranous coverings. The device can be attached to a delivery hub. The wires forming the occluder region and securing region can have a shape-memory capability such that they can be collapsed and distorted in a sheath during delivery, but resume and maintain their intended shape after delivery.

Abstract: An embolic coil which can be used for occlusive purposes in the vasculature is described. A mandrel for manufacturing a coiled structure, and method/process for manufacturing a coiled structure is described.

Abstract: Devices and methods are disclosed for occluding endovascular and non-endovascular defects, including parent artery occlusions, aneurysms and other abnormal openings in the body. The devices include one or more expandable braids that may be coupled to one or more helical coils suitable for introduction and retrieval from within a treatment area using a delivery catheter.

Abstract: A hemostatic device is provided to stop bleeding at a puncture site on the wrist of a patient, the device comprising a transparent flexible band to be wrapped at the site where the bleeding is to be stopped, a curved frame having an inner peripheral side and possessing a first curved portion in its first half and a second curved portion in its second half, a first balloon provided on the inner peripheral side in the first half of the curved frame and a second balloon provided on the inner peripheral side in the second half of the curved frame, the first balloon being larger than the second balloon. The bleeding from radial artery is stopped by compressing the radial artery at the puncture site using inflation of the first balloon and radial artery flow is increased by compression of ipsilateral ulnar artery using inflation of the second balloon.

Abstract: A hemostatic device is provided to stop bleeding at a puncture site on the wrist of a patient, the device comprising a transparent flexible band to be wrapped at the site where the bleeding is to be stopped, a curved frame having an inner peripheral side and possessing a first curved portion in its first half and a second curved portion in its second half, a first balloon provided on the inner peripheral side in the first half of the curved frame and a second balloon provided on the inner peripheral side in the second half of the curved frame. The bleeding from a first artery is stopped by compressing the first artery at the puncture site using inflation of the first balloon and the blood flow in the first artery is increased by compression of a second artery using inflation of the second balloon.

Abstract: A tourniquet for application to a patient's limb in an emergency situation, and a method for its application. The tourniquet includes a tension-sensing mechanism used to establish a baseline tension in a loop around an injured limb, and a tension-increasing mechanism to reduce the circumference of the loop and tighten the tourniquet as required beyond the baseline tension. The tension-sensing mechanism may be incorporated in a buckle in which when sufficient tension is developed in the loop a pin protrudes to engage and maintain tension in a strap member which is part of the loop. A latch may be incorporated in the buckle to keep it in a condition in which the pin protrudes to engage the strap and maintain the baseline tension. A release tab operable to release the latch is located where it is protected against inadvertent operation.

Abstract: The ultrasonic probe for a shoulder joint includes a curved extending section curved to a probe main body toward a first intersecting direction intersecting a longitudinal axis. The curved extending section includes a first curved outer surface facing the first intersecting direction, a second curved outer surface facing a second intersecting direction opposite of the first intersecting direction, a third curved outer surface facing a first width direction perpendicular to the first and second intersecting directions, and a fourth curved outer surface facing a second width direction opposite of the first width direction. A cutting surface on the second curved outer surface is different from a cutting surface on each of the third curved outer surface and the fourth curved outer surface in extending pattern of the grooves.

Abstract: A modular reaming system for reaming a plurality of pockets in an anatomical feature extends along a longitudinal axis. The system includes a first reamer in a first position on the longitudinal axis, and the first reamer reams a first pocket in the anatomical feature. The system further includes a second reamer that is removably coupled to the first reamer in a second position on the longitudinal axis. The second reamer reams a second pocket in the anatomical feature. The second reamer is keyed against rotation relative to the first reamer to ream the first and second pockets substantially simultaneously.

Abstract: An orthopedic reamer cutting tool is disclosed. The reamer is constructed having a hemispherical cutting shell that extends from an equatorial base to an apex. A plurality of cutting teeth, each having a primary tissue cutting surface, extend from the exterior surface of the cutting shell. A plurality of retractable blades, each having a secondary tissue cutting surface, are supported on a rotatable cam positioned at the base of the shell. Rotation of the cam in one of a clockwise or counterclockwise direction causes the retractable blades to extend through respective slits that extend through the thickness of the reamer shell. Rotation of the cam in the opposite direction causes the retractable blades to retract through the slits, back into the interior of the shell.

Abstract: Tissue removal probes comprise an elongated member, a drive shaft rotatably disposed within the member, and a rotatably tissue removal element mounted to the distal end of the drive shaft. One tissue removal element comprises a plurality of tissue-cutting filaments affixed at proximal and distal ends of the tissue removal element. The cutting filaments may have optional hinge points that allow the distal end of the tissue removal element to be inverted, thereby transforming the tissue removal element from a tissue-cutting device to a tissue-grasping device. Another tissue removal element may have a blunted tip to prevent distal tissue trauma and an irrigation port to provide irrigation fluid to the removed tissue and/or tissue removal element. Another tissue removal element has a proximal and distal spiral grooves that are oppositely pitched, so that removed tissue can be collected in the middle of the tissue removal element.

Abstract: Disclosed herein are systems and methods to remove material of interest, including blood clots, from a body region, including but not limited to the circulatory system for the treatment of pulmonary embolism (PE), deep vein thrombosis (DVT), cerebrovascular embolism, and other vascular occlusions.

Abstract: A device arranged to sustain and/or provide at least partial patency of a small blood vessel exhibiting an occlusion, the device constituted of a tubular body expandable from a first small diameter state for manipulation to, and through, the occlusion of the small blood vessel and a second large diameter state, the inner dimensions of the second large diameter state being no more than 50% of the diameter of the small blood vessel at the occlusion location, the device presenting a conduit for blood flow through the occlusion when in the large diameter state. In one embodiment the small blood vessel is an intracranial blood vessel.

Abstract: An inflatable device for insertion into a user's nose for controlling nasal exudation has an elongated shaft including at least one lumen for accommodating a fluid; an inflatable balloon connected to the shaft, the balloon being in fluid connection to the lumen; and an absorber for absorbing nasal exudates, the absorber being disposed at an outer circumference of the shaft and/or at a distal tip portion of the device. Another inflatable device for insertion into a user's nose for controlling nasal exudation has an elongated shaft including at least one lumen for accommodating a fluid; and an inflatable balloon connected to the shaft, the balloon being in fluid connection to the lumen; the balloon containing a cooling agent, wherein the cooling agent is configured to cool the balloon when coming into contact with the fluid.

Abstract: An electromechanical surgical system having an instrument housing for connecting with a shaft assembly, a shaft assembly, and an end effector. The end effector is an articulating end effector and the system includes a cable tensioning system for tensioning the articulation cables. The system includes a clutch mechanism for preventing slippage of a drive cable.

Abstract: A differential dissecting instrument for differentially dissecting complex tissue comprising is disclosed. The differential dissecting instrument comprises a rotary drive train having a central, longitudinal axis, a distal end, and a proximal end. The differential dissecting instrument also comprises at least one differential dissecting bluntwheel, wherein the at least one differential dissecting bluntwheel is rotatably associated with the distal end of the rotary drive train, has at least one axis of rotation substantially transverse to the central, longitudinal axis of the rotary drive train, and is rotated by the rotary drive train. The bluntwheel may comprise projections that are configured to differentially dissect a complex tissue when the differential dissecting instrument is in operation.

Abstract: The present application pertains generally to medical systems and methods for creation of an autologous tissue valves within a mammalian body. In some embodiments, a system for creating an endoluminal valve from a blood vessel wall is provided. The system includes a tubular assembly having a longitudinal axis, a proximal end, a distal portion with a distal end, and a first lumen extending from the proximal end to a distal port located proximate the distal portion. The distal portion can have a supporting surface that extends in a longitudinal direction and is offset from a surface of the tubular assembly proximal the distal port. The system can further include a tissue dissection probe disposed within the first lumen.

Abstract: A method and apparatus for transecting soft tissue, such as a ligament, and more particularly, the transverse carpal ligament. A pair of hollow introducer needles can be used to rout a thread-like, smooth and non-abrasive cutting element around tissue, such as a soft tissue, to enable a transection of the soft tissue using minimally invasive techniques. The cutting element is routed into position about the target soft tissue such that the cutting element both enters and exits the body from the same side of the soft tissue. The smooth and non-abrasive exterior surface of the cutting element serves to provide a kerf-less cut.

Abstract: A tissue resection device for resecting tissue from a target site within a patient's body. The device includes an elongate shaft having a proximal end and a distal end. An actuation member extends partially through the shaft, and reciprocates within the shaft between a retracted position and an extended position. Multiple snare wires extend through the actuation member, and emerge outwards from a distal portion of the actuation member. The snare wires cooperate and join to form a snare loop, which engages the tissue intended to be resected. The snare loop is configured to enhance friction while engaging the tissue, to resect the tissue.

Abstract: An ultrasonic probe treating a shoulder joint includes a probe main body section extended along a longitudinal axis, and a curved extending section extended in a state of curving relative to the probe main body section toward a first intersecting direction side when a certain direction intersecting the longitudinal axis is defined as the first intersecting direction. The curved extending section includes a first curved outer surface facing the first intersecting direction side, and a second curved outer surface facing a second intersecting direction side when an opposite direction of the first intersecting direction is defined as the second intersecting direction. An acute angle of a tangent line at a distal end of the second curved outer surface relative to the longitudinal axis direction is 20° or more and 25° or less.

Abstract: The ultrasonic probe for a shoulder joint includes a curved extending section curved to a probe main body toward a first intersecting direction intersecting a longitudinal axis. The curved extending section includes a first curved outer surface facing the first intersecting direction, a second curved outer surface facing a second intersecting direction opposite of the first intersecting direction, a third curved outer surface facing a first width direction perpendicular to the first and second intersecting directions, and a fourth curved outer surface facing a second width direction opposite of the first width direction. A relay groove on a cutting surface in the second curved outer surface is continuous with extending grooves on cutting surfaces in the third curved outer surface and the fourth curved outer surface.

Abstract: The present application pertains generally to medical systems and methods for creation of an autologous tissue valves within a mammalian body. In some embodiments, a system for creating an endoluminal valve from a blood vessel wall is provided. The system includes a tubular assembly having a longitudinal axis, a proximal end, a distal portion with a distal end, and a first lumen extending from the proximal end to a distal port located proximate the distal portion. The distal portion can have a supporting surface that extends in a longitudinal direction and is offset from a surface of the tubular assembly proximal the distal port. The system can further include a tissue dissection probe disposed within the first lumen.

Abstract: A holding mechanism includes an opening portion through which the guide member is inserted in a bending state. The mechanism includes a gap portion which has a cutout surface that is provided by cutting out one part of the holding mechanism in a radial direction of a central axis of an insertion opening portion, and that guides the guide member into the opening portion from the insertion opening portion. The mechanism includes a lock mechanism which is provided in the radial direction and which locks the guide member inserted through the opening portion at two places different from each other in positions in the central axis direction of the insertion opening portion so that one part of the guide member maintains the bending state.

Abstract: Methods of providing sympathetic nerve blocks comprise inserting a portion of a catheter into a subject. A distal end of the catheter is positioned on a lateral side of at least one vertebra of a vertebral column of the subject proximate to a portion of a sympathetic nervous system of the subject. A medication is supplied through the catheter to effect a sympathetic nerve block in the subject. Methods of alleviating pain in lower extremities of subjects comprise inserting a portion of a catheter into a subject and supplying a medication through the catheter. Catheters and catheter assemblies may be used in administering such sympathetic nerve blocks. Catheters and catheter assemblies may be used in administering medication to one or more of a peripheral nervous system of a subject and a spinal cord of a subject.

Abstract: A treatment instrument insertion assisting tool is provided with: a connection portion configured to be connected to a channel of a tool inserted into a subject; an introduction port for a treatment instrument inserted into the channel via the connection portion; a cylindrical guiding portion tapered from the introduction port to the connection portion; and a plurality of recess portions provided on an outer circumferential edge of the introduction port, each of the recess portions having such a shape that gradually increases in width from the connection portion side toward the introduction port side and that is recessed toward the connection portion side.

Abstract: An access device for placing a medical article within a body space includes a needle, a dilator, and a sheath. The dilator can be coaxially and slideably disposed about the needle, and the sheath can be coaxially and slideably disposed about the dilator. The access device can further include a inner member coaxially disposed between the needle and dilator. The needle can include a fenestration in fluid communication with a space between the needle and inner member. When the needle punctures a blood vessel, the fenestration allows blood to flow into the space between the needle and inner member to provide a visual indicator to a physician or healthcare professional that the needle is in a vessel.

Abstract: Embodiments may include an expandable access system having contracted and expanded configurations. The system and methods may include an expandable access device having a helix or wrapped shape. Embodiments may include a cannula, stent, needle, trocar, introducer, fastener, and/or any other devices disclosed herein. Embodiments may also include an expandable trocar positionable in at least a portion of the access device. A sleeve or band may be disposed over at least a portion of the access device and configured to resist radial expansion of the access device. Expansion of the trocar and/or receipt of an object may radially expand the access device between a contracted configuration and an expanded configuration.

Abstract: A tattoo ink or colorant has magnetic properties. The ink is delivered to the proper depth of the skin. The colorant remains in place, forming the desired visible design. When removal of the tattoo is desired, a magnet is topically applied to draw the ink or colorant to move the nanoparticles to the epidermis. The nanoparticles are then shed from the epidermis along with squamous cell debris.

Abstract: A uniplanar pedicle fastener that is bottom-loaded and has a two-part pivoting mechanism is provided. The bottom loading is effected by particular complementary shapes of the fastener head and an opening in the bottom of the housing. The pivoting mechanism is provided by a protrusion and recess in the fastener head and housing bottom, respectively. The complementary dimensions of the fastener head, protrusion, housing opening, and recess permit both the bottom loading at one orientation, and, at a second generally perpendicular orientation, the pivoting articulation. The uniplanar pedicle fastener of the present invention can be attached to other pedicle fastener assemblies as part of a spinal stabilization apparatus.

Abstract: An orthopedic connection assembly is described that comprises a housing member for receiving an implant that is operably connected to a receiving member for receiving an anchor member. The connection assembly is configured to have a locking mechanism that secures and fixes the relative orientation between the implant and the anchor member. The connection assembly can comprise a plate member receivable within the housing member. When a securing member such as a set screw is introduced downwardly into the housing member to secure the implant, the securing member applies a lateral force to the plate member, which presses against an interference member within the receiving member. The interference member presses against the anchor member, such that the anchor member is fixed in a position relative to the implant.

Abstract: A spinal fixation device is provided having first and second elongate members that are angularly adjustable relative to one another. Each elongate member can include a connecting feature formed on a terminal end thereof, and each connecting feature can be coupled to one another to allow angular movement of the first and second elongate members. The device can also include a locking mechanism that is adapted to couple to the connecting feature on each of the first and second elongate members to lock the elongate members in a fixed position relative to one another.

Abstract: A device for connecting two spinal rods is provided. In one form, the device includes two clamping devices for receiving and locking to spinal rods and a central bridge or plate member that couples the clamping devices. In one aspect, the clamping devices are unitary members with deflectable jaw portions that snap-fit and then locked by operation of actuators. In another aspect, one or both of the clamping devices are adjustably coupled to the central bridge or plate member to allow at least translation and pivoting or rotation of the clamping devices relative to a central axis of the elongate bridge member. The clamping devices may be coupled to the bridge or plate member with the same locking actuator that causes clamping of the clamp device so that the positions of the clamp device and the spinal rod are locked into place by manipulation of only a single locking actuator.

Abstract: A method of implanting a spinal implant device. The method includes removing a portion of a superior spinolaminar junction and an inferior spinolaminar junction. The method includes removing a portion of each facet joint. The method includes providing the spinal implant device including a fusion cage having a superior saddle portion, an inferior saddle portion and opposing cage ends. The method includes positioning the fusion cage between spinous processes with the superior saddle portion receiving the superior spinolaminar junction where the portion of the superior spinolaminar junction having been removed, the inferior saddle portion receiving the inferior spinolaminar junction, and opposing cage ends respectively contacting the opposing facet joints.

Abstract: A spinal stabilization system and method are provided for treating a patient's spinal column, for maintaining preselected spacing and movement between adjacent vertebrae in a spinal column, and for providing overall stability thereto. The system includes interlaminar members positioned in the spaces intermediate a first vertebra and the vertebrae positioned immediately above and immediately below and adjacent to the first vertebra. The interlaminar members are operatively connected to one another by an adjustable support structure and cooperate therewith to maintain the preselected spacing between adjacent vertebrae and to provide overall stability to the spinal column.

Abstract: A spinal joint distraction system for treating a facet joint including articular surfaces having a contour is disclosed and may include a delivery device including a generally tubular structure adapted to engage a facet joint, an implant adapted to be delivered through the delivery device and into the facet joint, the implant comprising two members arranged in opposed position, and an implant distractor comprising a generally elongate member adapted to advance between the two members of the implant causing separation of the members and distraction of the facet joint, wherein the implant is adapted to conform to the shape of the implant distractor and/or the articular surfaces of the facet upon being delivered to the facet joint. Several embodiments of a system, several embodiments of an implant, and several methods are disclosed including a method for interbody fusion.

Abstract: A multi-layer, fiber-reinforced composite orthopaedic fixation device having a design selected based on a desired characteristic of the orthopaedic fixation device. The design may be selected according to a model of the device, the model defining design constraints, and the design may comprise a pattern of the fiber angle for each layer. The selection of a design may be analyzed using finite element analysis to determine whether the design will comprise the desired characteristic.

Abstract: A bone transport system includes a nail having a proximal end and a distal end, the proximal end configured for securing to a first portion of bone, the distal end configured for securing to a second portion of bone. The system includes a housing having a wall with a longitudinal opening extending a length along a portion thereof. The system further includes a transport sled having a length that is shorter than the length of the longitudinal opening, the transport sled configured for securing to a third portion of bone, the transport sled further configured to be moveable along the longitudinal opening. The system further includes a magnetic assembly disposed within the nail and configured to be non-invasively actuated by a moving magnetic field, wherein actuation of the magnetic assembly moves the transport sled along the longitudinal opening. The system further includes a ribbon extending on opposing sides of the transport sled and substantially covering the longitudinal opening.

Abstract: An intramedullary bone fixation device is disclosed herein. The device includes a first longitudinally extending member, a second longitudinally extending member, and a coupling member. The first longitudinally extending member includes a connector end and a bone engagement end opposite the connector end. The second longitudinally extending member includes a connector end and a bone engagement end opposite the connector end. The coupling member is configured to engage the connector ends of the respective longitudinally extending members, thereby coupling the first longitudinally extending member to the second longitudinally extending member. The device may be provided in an kit form at least partially unassembled. The device may be delivered into a fracture and fully assembled within the fracture or adjacent bone via percutaneous or minimally invasive surgical procedures. The device, on account of its configuration and assembly, may be considered modular in some cases.

Abstract: A reversible bone coupling device including a first component having a first elongated stem portion for insertion from a first end longitudinally into a surface of a first bone piece, and a second component having a second elongated stem portion for insertion from a second end longitudinally into a surface of a second bone piece, and a connector extending from a second top for coupling with the first component and reversibly locking therein.

Abstract: A method includes inserting a first surgical device into an exposed first end of a first bone until a trailing end of the first surgical device is disposed adjacent to the first end of the first bone. A second surgical device is inserted into an exposed first end of a second bone while the first surgical device remains disposed within the first bone. A first portion of an implant is advanced into the second bone while being engaged with a passageway defined by the implant such that the implant is guided by the second surgical device. The second surgical device is removed from the second bone and from its engagement with the implant. The first bone is repositioned such that the first surgical device is aligned with the passageway defined by the implant, and the first bone is forced into engagement with a second portion of the implant.

Abstract: An intramedullary implant system, and method for placement within a bone system are provided by the invention. The implant includes a body with at least one pair of beams arranged about a longitudinal axis of the body. The beams are each fixed to the body and each have an end. The end of one of the beams of a pair is releasably coupled to the other beam of the pair by a k-wire from one end of which extends a flexible tail. The beams are each deflectable between (i) a coupled and biased position for insertion of the beams into a respective bone, and (ii) an uncoupled position for gripping bone. The beams of each pair in the uncoupled position being arranged so as to compressively engage the bone.

Abstract: An implant kit has an adapter having a first end, a second end, and a longitudinal axis extending from the first and to the second end, wherein the first end is configured for removably receiving and engaging an implant and the second end is configured for removably coupling to a driver shaft of an implant driving tool, and an implant preloaded into the first end of the adapter, the implant having an elongated threaded portion; and a blade portion extending from the elongated threaded portion, and having two serrated edges, wherein the blade portion is received in the first end of the adapter and the elongated threaded portion of the implant is coaxially aligned with the longitudinal axis of the adapter.

Abstract: A system, devices and methods are provided for facilitating stabilization of periarticular fractures. The system includes a compression plate and one or more of a cerclage cable for encircling the bone and securing the compression plate to the bone, a crimp lug for securing the cable in tension relative to the bone and/or a plate, and a supplemental plate coupled to the compression plate and adapted to receive bicortical or unicortical bone screws to further secure the compression plate relative to the bone. In addition, the system includes a cable tensioner for temporarily retaining the cable in tension and then applying a tension to the cable until a desired compression is effected between a plate and bone and while a cable retaining structure is secured to the cable to retain the applied tension on the cable. Also provided is a jig for use with plates for minimally invasive fracture stabilization.

Abstract: Bone plates having an adjustable joint, and methods of using the bone plates to fix bones.

Abstract: A bone fixation plate, comprises an elongated body contoured to conform to the anatomy of a clavicle, the elongated body comprising a head at a first end and a shaft extending therefrom to a second end, the second end further comprising a reduced diameter tapered tip configured to permit insertion of the elongate body through a minimally invasive incision formed adjacent the clavicle. The bone fixation plate also comprises a first plate hole extending through the shaft from a proximal face to a distal face, the first plate hole formed as a combination hole and a second plate hole extending through the head from the proximal face to the distal face, the second plate hole being threaded.

Abstract: The present invention relates to a fixing tool for an open-wedge high tibial osteotomy, and a fixing tool for an open-wedge high tibial osteotomy, which is installed on a tibia cut open due to a tibial osteotomy, includes: a fixing plate which includes a head portion that has a plurality of nut holes, and an elongated plate that has a plurality of nut holes and a long hole and is formed to protrude from one side of the head portion; screws which are coupled to the nut holes; and a block which is detachably installed in the long hole by using a fixing screw. Therefore, the fixing tool is closely fixed to a tibia, which has been cut open due to a procedure of a high tibial osteotomy, thereby enabling solid union of the tibia.

Abstract: Disclosed herein is a bone fixation device. The fixation device has a head portion having a conduit and a plurality of pawls formed therein along one side of the conduit; and an elongation strip having a hooked end and a plurality of ratchet teeth formed thereon the body of the strip. The head portion is connected to the non-hooked end of the elongation strip at an angle between 100-170 degrees, and the plurality of pawls of the head portion engage the plurality of teeth when the elongation strip is inserted into the conduit of the head portion to form a loop around the weaken or fractured bone so as to stabilize the weaken or fractured bone.

Abstract: A woven retention device can include a pair of connected opposing lattice segments comprising intersecting filaments. The pair of connected opposing lattice segments can be configured to be placed in a portion of a circumference of a bone hole of a bone. A method of inserting a woven retention device can include inserting a woven retention device into a bone hole of a bone. The inserting the pair of opposing lattice segments can cover only a portion of a circumferential area of the bone hole. The method can include securing a fastening device into the bone hole having the inserted woven retention device. Upon securing the fastening device into the bone hole, a portion of the fastening device interfaces directly with the surface of the bone in the bone hole and a portion of the fastening device can interface directly with the bone interface of the woven retention device.

Abstract: A soft tapping device for preparing a bone hole that includes a substantially cylindrical insert that is sized to enter into a compressed woven retention device. The substantially cylindrical insert has protrusions that are adaptable to expand portions of a compressed woven retention device inside the bone hole. The substantially cylindrical insert is also configured to exit from the compressed woven retention device without changing the expanded portions of the compressed woven retention device.