Abstract: A surgical stapler includes a first elongate member having a distal portion that supports a plurality of staple-forming pockets, a second elongate member having a distal portion that supports a staple cartridge, and a clamp member movable from an open position to a closed position to releasably clamp the first and second elongate members together. A clamp lockout feature is supported by the first elongate member and is moveable between a lockout position in which the clamp lockout feature prevents closure of the clamp member, and a release position in which the clamp lockout feature permits closure of the clamp member. An actuating feature is supported by the second elongate member and is configured to actuate the clamp lockout feature from the lockout position to the release position in response to approximation of the distal portions of the first and second elongate members.

Abstract: The present disclosure relates to a surgical fastener applying apparatus for applying fasteners to body tissue. The apparatus includes a cartridge receiving half-section defining an elongated channel member configured to releasably receive a firing assembly and a single use loading unit. A lockout structure prevents insertion of the single use loading unit into the channel member after the firing assembly is mounted to the cartridge receiving half-section. Alternatively, the lockout structure prevents full insertion of the firing assembly into the cartridge receiving half-section, if the single use loading unit is not engaged with the firing assembly.

Abstract: A surgical suturing apparatus includes an end effector including a jaw assembly and a needle assembly. The jaw assembly includes first and second jaws movable between open and closed positions. Each of the first and second jaws includes a tissue facing surface having an elongated rail and a longitudinal row of teeth. Each tooth of the longitudinal rows of teeth of the first and second jaws includes a needle channel extending therethrough. The elongated rails and the longitudinal rows of teeth of the first and second jaws are disposed in opposed relation relative to each other. The needle assembly includes a first needle, a second needle, and a suture coupled to the first and second needles. The first needle is slidable through the needle channels of the first jaw and the second needle is slidable through the needle channels of the second jaw.

Abstract: An apparatus includes a handle assembly having a body, a shaft assembly having an outer tubular member extending distally from the body, an end effector, an anvil, and a trocar latch assembly. The end effector includes a staple deck fixed relative to the outer tubular member, a staple driver that can actuate relative to the staple deck between an unfired position and a fired position, and a trocar that can actuate relative to the staple deck and the staple driver, the anvil can couple with trocar to move relative to the staple deck to define a gap distance. The trocar latch assembly includes a locking body that can actuate between an unlocked configuration and a locked configuration in response to the staple driver actuating between the unfired position and the fired position. The locking body can selective fix the trocar relative to the staple deck in the locked position.

Abstract: An apparatus includes a handle assembly having a body, a shaft assembly having an outer tube member, an end effector, an anvil, a first trocar closure system, and a second trocar closure system. The end effector has having a staple deck fixed relative to the body, a staple driver operable to actuate relative to the staple deck between an unfired position and a fired position, and the trocar configured to selectively couple with the anvil and actuate relative to the staple dreck. The first trocar closure assembly can actuate in a first motion to drive the trocar between a distal position and a first closed position. The second trocar closure assembly can actuate in a second motion between the first closed position and a second closed position.

Abstract: An apparatus includes a body assembly with a handle and a shaft portion, an end effector with a staple deck fixed to the shaft portion, an anvil, and a firing assembly. The end effector further includes a trocar and a staple driver both configured to actuate relative to the staple deck. The staple driver can actuate a distance between an unfired position and a fired position. The trocar can couple with the anvil to define a gap distance. The firing assembly includes a trigger pivotably coupled with the body assembly via a first pivot, a driver actuator configured to actuate the staple driver, and a linkage assembly pivotably coupled with the trigger via a second pivot and the driver actuator. Where the second pivot is proximal relative to the first pivot. The linkage assembly can drive the driver actuator is response to the trigger pivoting about the first pivot.

Abstract: A clip treatment tool includes: a clip body that has two arm portions and a folded portion, the two arm portions, the folded portion connecting proximal end parts of the two arm portions; a tightening ring that functions to close the two arm portions in accordance with movement of the clip body from a distal end side toward a proximal end side; a pressing tube that has at least one opening formed in an outer surface thereof, and that allows the clip body to be contained therein in accordance with the movement of the clip body; and a coupling member that has a distal end part to which the folded portion is removably connected and a proximal end part to which a distal end part of an operation wire is fixed, the coupling member coupling the clip body and the operation wire to each other.

Abstract: Surgical clip appliers are provided and includes a channel assembly extending distally from a housing; a clip carrier disposed within said channel assembly and defining a channel and a plurality of windows therein; a plurality of clips slidably disposed within said channel of said clip carrier; a wedge plate reciprocally disposed within said channel assembly, said wedge plate being operatively connected to said handles and including a plurality of apertures formed along a length thereof; and a clip follower slidably disposed within said channel of said clip carrier and disposed proximally of said plurality of clips, said clip follower being configured and adapted for selective engagement with said windows of said clip carrier and said apertures of said wedge plate. The clip follower is configured and adapted to urge said plurality of clips, in a distal direction relative to said clip carrier, upon reciprocal movement of said wedge plate.

Abstract: A gastroesophageal reflux preventer and related methods are provided. The gastroesophageal reflux preventer may include an absorbable material able to be placed in contact with a body organ and configured to induce a scarification of the body organ in response to absorption by the body organ of the material. In this manner, a proximate sphincter may be tightened, such as to ameliorate reflux through a gastroesophageal sphincter.

Abstract: A vaso-occlusive device delivery assembly includes a pusher assembly having proximal and distal ends, a conductive sacrificial link disposed at the distal end of the pusher assembly, and a vaso-occlusive device secured to the pusher assembly by the sacrificial link. The pusher assembly includes first and second conductors extending between the proximal and distal ends thereof. The sacrificial link is electrically coupled between the first and second conductors, such that the first conductor, sacrificial link and second conductor form an electrical circuit, and, when a disintegration current is applied through the sacrificial link through the first and second conductors, the sacrificial link thermally disintegrates, thereby releasing the attachment member and vaso-occlusive device from the pusher assembly.

Abstract: A clip treatment tool includes a clip body that has two arm portions and a folded portion, the folded portion connecting proximal end parts of the two arm portions; a pressing tube that allows the clip body to be contained therein in accordance with movement of the clip body from a distal end side toward a proximal end side; a coupling member that couples the clip body and an operation wire to each other; and an urging member that urges the coupling member relative to the pressing tube from the proximal end side toward the distal end side. The pressing tube has a latched portion, and the coupling member has a latch portion. In accordance with movement of the operation wire from the distal end side toward the proximal end side, the latch portion is latched to the latched portion, and the coupling member is locked to the pressing tube.

Abstract: The present disclosure relates to a ligation device, an unlocking method, and a ligation instrument. The ligation device may include a clip and a limiting tube. A distal end of the clip may be used for ligation. The limiting tube may be provided with an accommodation channel, and a proximal end of the clip may be connected with the accommodation channel, and the proximal end of the clip may move into or out of the limiting tube. The clip may be provided with a locking portion, and the limiting tube may be provided with a locking position that is matched with the locking position. When the locking portion is locked with the locking position, the locking portion may be unlocked from the locking position by operating the locking portion. Alternatively, the clip may be provided with an unlocking portion that is coupled with the locking portion. The locking portion may be unlocked from the locking position by operating the unlocking portion.

Abstract: An airway valve apparatus 10 for at least partially sealing an airway 30 of a subject 40 comprising: a hub 50; a plurality of anchor struts 60 disposed about and in communication with the hub; a plurality of support struts 70 disposed about and in communication with the hub; one or more membranes that are in communication with the plurality of anchor struts, the plurality of support struts, or both; and wherein the anchor struts include one or more anchor elements 62 disposed at a distal end of the anchor struts, the one or more anchor elements configured to engage a wall 32 of the airway.

Abstract: An apparatus for performing a vascular treatment is disclosed. In some embodiments, the apparatus comprises two modules that are maintained in separate zones of an operating environment. The apparatus includes an elongate, intraluminal member that is shaped and dimensioned for passage through blood vessels of a subject. The intraluminal member has a proximal end and a distal end. A vein wall disruptor for degrading the integrity of the inner wall of a vessel is housed within a sheath of the intraluminal member. The disruptor includes at least one, but may include several, prongs. The distal ends of the prongs contact or communicate with the inner wall of a blood vessel. The disruptor can include a contacting tip designed to damage the interior of the vessel as the disruptor is pulled proximally therealong. The apparatus further includes an automatic injector to inject a sclerosant into the blood vessel.

Abstract: Devices can generally include an implant having a braided section that can be implanted in a deployed state such that, in the deployed state, the braided section folds to form an outer occlusive sack extending across a neck of an aneurysm to engage a wall of the aneurysm from within a sac of the aneurysm and an inner occlusive sack forming a trough nested within the outer occlusive sack. The implant can be closed at one or more of the braid ends to define a substantially enclosed bowl-shaped volume.

Abstract: An apparatus for performing a vascular treatment is disclosed. In some embodiments, the apparatus comprises two modules that are maintained in separate zones of an operating environment. The apparatus includes an elongate, intraluminal member that is shaped and dimensioned for passage through blood vessels of a subject. The intraluminal member has a proximal end and a distal end. A vein wall disruptor for degrading the integrity of the inner wall of a vessel is housed within a sheath of the intraluminal member. The disruptor includes at least one, but may include several, prongs. The distal ends of the prongs contact or communicate with the inner wall of a blood vessel. The disruptor can include a contacting tip designed to damage the interior of the vessel as the disruptor is pulled proximally therealong. The apparatus further includes an automatic injector to inject a sclerosant into the blood vessel.

Abstract: Flexible air bladders and associated air assemblies provide compression and blood flow moderation in a variety of applications including blood flow restriction training (BFR) and limb compression for injury prevention. An integrated air assembly comprises a flexible manual pump, a check valve air intake, one-way valve and a pressure release valve. The user can properly position and fasten the air bladder around a limb using a special type of band, sleeve, or by wearing a piece of clothing containing strategically placed air bladders and integrated air assemblies. Each air assembly allows the user to easily and manually add air to the bladder by pressing on a designated area of the pump which causes the bladder to extend on the inward facing portion of the band, compression sleeve, or piece of clothing toward the limb until a desired pressure is achieved around the limb to support blood flow moderation.

Abstract: A radial artery compression band is disclosed for circumferential placement around the wrist of a patient to apply hemostasis pressure to a wound, which includes a first arcuate band portion including a radially outwardly extending support frame, a second elongated band portion including a plurality of longitudinally spaced apart radially outwardly extending ramped engagement teeth, a third elongated band portion extending between the first and second band portions and including a radially inwardly facing compression structure for applying hemostasis pressure to the wound, and a band adjustment mechanism mounted within the support frame of the first arcuate band portion and including an axially rotatable shaft having a worm gear section with a continuous helical thread for selectively intermeshing with the ramped engagement teeth on the second elongated band portion to adjust band tension through axial rotation of the shaft.

Abstract: Disclosed herein is a fluid management assembly. The fluid management assembly includes a handpiece, a slider based fluid control mechanism, and a fluid occluding member. The slider based fluid control mechanism housed in the handpiece. The fluid occluding member is configured to be in communication with the fluid control mechanism. The fluid occluding member being separate from the handpiece.

Abstract: A wedge osteotomy device including a cutting guide coupled to a base plate via a joint. The cutting guide configured to pivot relative to the base plate about a pivot axis extending through the joint. The cutting guide including a guide body including a cutting slot extending through the guide body, an arcuate slot extending through the guide body and defining a radius to the joint, and a plurality of markers on the guide body identifying a position of the cutting guide relative to the base plate. The base plate including planar top and bottom surfaces.

Abstract: A surgical dissection tool for cutting bone and other tissue includes a cutting head having an outer surface having non-paired or an odd number of flutes formed therein. Each flute includes a rake surface intersecting with the outer surface to form a cutting edge, and a relief surface opposite the rake surface. The relief surface and the rake surface form a first angle. Each flute also includes a leading angled surface extending from the relief surface to a distal end portion of the cutting head, the leading angled surface and the rake surface forming a second angle substantially the same as the first angle.

Abstract: A surgical system including a surgical tool and a navigation system for tracking the position of the surgical tool. The surgical tool comprising a housing including a variable speed motor and control module disposed within the housing. The navigation system comprising a navigation console in communication with the control module of the surgical tool, the navigation console may be configured to communicate instructions to the control module of the surgical tool based on the position of the surgical tool relative to a defined zone. The navigation console may be configured to deactivate the surgical tool based on the position of the surgical tool relative to the defined zone. The navigation console may also be configured to provide a user-selectable override option to allow continued operation of the surgical tool within the defined zone.

Abstract: Systems and methods related to use of a measurement system in conjunction with a powered instrument for determination of the placement of a tool portion relative to the anatomy of a patient utilizing the powered instrument. The measurement system may include a displacement sensor that indicates the relative displacement of the tool portion relative to the anatomy. The system may also include a sensor for monitoring a tool drive signal representative of a tool drive parameter that is characteristic of the tool portion acting on the anatomy. The tool drive signal may be analyzed relative to a given amount of axial displacement as measured by the displacement sensor to avoid false indications of placement based on noise and or other artifacts in the tool drive signal that may result from characteristics of the anatomy and/or operational behaviors of the surgeon utilizing the instrument.

Abstract: A reamer shaft extension includes a shaft positioned between a first end having a first coupling and a second end having a second coupling. The first coupling of each reamer shaft extension is selectively couplable with the second coupling of another reamer shaft extension such that a select amount of reamer shaft extensions are assembled together to form a reamer shaft extension assembly for use in a reaming procedure. Each reamer shaft extension further has a sufficiently short enough length such that each reamer shaft extension is insertable within a sterilization tray for use in a sterilization procedure.

Abstract: An anchor delivery system includes both a straight and curved drill guide along with a flexible drill, a flexible obturator and a flexible anchor inserter. The curved drill guide has a distal tip with approximately a 15° bend from the primary axis of the drill guide. Both the drill and the obturator have a reduced diameter section to improve flexibility during passage through the curved drill guide. Additionally, a surface of the inserter shaft has a laser cut pattern which permits flexing of the inserter around the inner diameter of the curved drill guide.

Abstract: An aspiration device can be used to aspirate an obstruction from a blood vessel. The aspiration device is configured to allow controlled one-handed aspiration yet maintain a syringe plunger feel of vacuum. The aspiration device also allows one-handed injection to empty the device when needed. Furthermore, mechanisms enable one-handed locking of a plunger position of the device to maintain vacuum when the user releases the device.

Abstract: A clot retrieval device is provided. The clot retrieval device includes a capturing basket having an opening at a proximal end where the capturing basket is deployable downstream from a clot in a blood vessel. The capturing basket is configured to surround a portion of the clot and the opening in the proximal end of the capturing basket is configured to reduce in size such that the capturing basket conforms around the portion of the clot and be retrieved after the capturing basket conforms around the portion of the clot.

Abstract: The tissue retrieval system deploys a tissue bag at the surgical site. The bag is supported by the system as tissue is placed within the bag and is closed to isolate the collected tissue and allow the bag and collected tissue to be removed from the body. The bag can be reopened and re-closed as desired through use of a guide bead and cord. The bead also facilitates removal of the collected tissue.

Abstract: A medical device, configured to perform an endovascular therapy, e.g., thrombectomy, can comprise an elongate manipulation member having a first connection member proximate a distal end of the elongate manipulation member, and an intervention member having a second connection member proximate a proximal end of the intervention member. The second connection member can be connected to the first connection member such that the first connection member can rotate relative to the second connection member.

Abstract: A surgical instrument system includes a main body having a handle and a drive assembly. The drive assembly includes a plurality of gears and rotation transfer mechanisms for translating the movements of the handle into a mechanical force. A surgical tool having a tool body, an elongated shaft and an effector assembly is removably engaged to the main body of the system. The tool body houses a transfer gear assembly for engaging the drive assembly. A plurality of control wires extends from the transfer gear assembly to the effector assembly. The effector assembly includes a frame member having a pair of arms positioned along the distal end. The arms functioning to selectively open, close and move omnidirectionally based on an input of the handle.

Abstract: Devices and methods for processing animal or human tissue are provided. The devices may include a rod having a central axis and configured to simultaneously rotate around the central axis and move along the central axis. The device can further include a group of blades which are attached to the rod and positioned proximate the rigid support surface.

Abstract: Disclosed is a surgical device. The surgical device includes a housing. The surgical device also includes a linear actuator disposed in the housing. The linear actuator includes a central rod. The linear actuator also includes one or more bending modules connected to the central rod. Each of the one or more bending modules includes one or more bending actuators. Each of the one or more bending actuators includes one or more layers of piezoelectric bending elements configured to provide a reciprocating movement to the central rod upon application of a voltage. The surgical device further includes a cutting mechanism coupled to the central rod.

Abstract: A surgical instrument includes a hollow member having a sidewall provided with a window and a closure member movably connected to the hollow member for alternately covering and uncovering the window. The hollow member has a first clamping surface along an edge of the window, while the closure member has a second clamping surface opposing the first clamping surface and disposable substantially adjacent thereto in a clamping or closure configuration of the instrument. The instrument additionally comprises a tissue occlusion component mounted to at least one of the hollow member and the closure member for acting on tissues gripped between the first clamping surface and the second clamping surface, to couple the tissues to each other.

Abstract: The disclosed technology is directed to an ultrasonic probe comprises a probe main portion configured to transmit ultrasonic vibration generated by an ultrasonic transducer. A treatment portion is configured on a distal side of the probe main portion along a longitudinal axis thereof. The treatment portion includes first direction surfaces disposed in a first direction intersecting the longitudinal axis and second direction surfaces that are adjacent to the first direction surfaces and are disposed in a second direction different from the first direction surfaces. The first direction surfaces further includes a plurality of surfaces formed into a staircase shape when being viewed from the treatment portion and one or more surfaces formed into a staircase shape when being viewed from a side opposed to the distal side of the treatment portion. The second direction surfaces further includes a plurality of surfaces formed into a staircase shape toward the distal side.

Abstract: A needle guide to retain a needle at a desired trajectory with respect to an imaging transducer includes a body member, a needle holder subassembly, and a slide member. The needle holder subassembly is pivotably mounted on the body member to enable the needle holder subassembly to be oriented to various selected orientations with respect to the body member. The slide member is slidably coupled to each of the body member and the needle holder subassembly, such that movement of the slide member relative to the body member moves the needle holder subassembly between the various selected orientations.

Abstract: Devices used to provide transseptal access are disclosed. The devices may comprise at least one cannula, a needle, and a handle. The cannula and the needle may be configured to be inserted through a dilator while not damaging a lumen wall of the dilator. The handle may be configured to lock the needle in a retracted position. The devices may be configured to telescopically advance the needle through an atrial septum.

Abstract: A surgical access device including a cannula, a seal, and a seal guard is disclosed. The cannula includes a housing and an elongated portion extending distally from the housing. The seal is disposed at least partially within the housing of the cannula and includes an aperture for sealed reception of a surgical instrument therethrough. The seal guard is disposed at least partially within the housing of the cannula and proximally of the seal. The seal guard is formed from a flat sheet of material and folded into a funnel-like shape.

Abstract: According to a general aspect, an insertion device includes an elongate member defining a lumen, a handle member movably coupled to the elongate member, a plunger member, at least a portion of the plunger member being disposed within the lumen defined by the elongate member, and an actuation member operatively coupled to the plunger member, the plunger member being configured to move from a first position within the lumen to a second location within the lumen in response to the actuation member being actuated.

Abstract: Systems, methods, and kits for performing endoscopic fusion with neuromonitoring. The endoscopic fusion may be performed, for example, through a cannula providing a portal to the disc space. Throughout various steps in the procedure, neuromonitoring may occur to minimize the possibility of injuring or contacting a nerve.

Abstract: A valve assembly for use with a surgical instrument is disclosed. The valve assembly includes a housing and a seal assembly disposed within the housing, the seal assembly including a septum seal including an orifice configured to sealingly engage a surgical instrument inserted therethrough, at least a portion of the septum seal defining a seal curvature, a first guard member including a plurality of curved first guard portions defining slits therebetween, and a second guard member including a plurality of curved second guard portions defining slits therebetween. The first and second guard members may be positioned in an overlapping relationship with the plurality of first guard portions rotationally offset with respect to the second guard portions. The wide, triangular shaped slits of the guard members may improve flexibility of the guard portions.

Abstract: An example implantable medical device (IMD) retrieval system may include an elongate outer tubular member including a longitudinally extending lumen terminating in a distal cup that is configured to receive the IMD; and a retrieval assembly including a retrieval member that includes an elongate member terminating in at least one snare that is moveable between an expanded configuration and a contracted configuration; and a fixed-curve catheter that includes a resilient material forming a distal curve and defining a lumen in which the retrieval member extends in sliding engagement, where the fixed-curve catheter extends in sliding engagement within the lumen of the elongate outer tubular member.

Abstract: A surgical instrument comprises a first member defining a cavity and including a locking surface disposed with the cavity. The locking surface is engageable with a longitudinal member to fix a tether with the first member. A second member includes an inner surface that defines a longitudinal passageway configured for disposal of a surgical driver engageable with a spinal construct. The second member further includes at least one mating element being engageable with the spinal construct. An actuator is connected with the members and is configured to incrementally tension the tether. Systems, implants and methods are disclosed.

Abstract: A vertebral column correction system for correcting a spinal deformity without fusing the joint segments is disclosed. The vertebral column correction system may have first and second vertebral anchors secured to first and second vertebrae. The vertebral column correction system may further comprise one or more intermediate vertebral anchors secured to vertebrae between the first and second vertebrae. A connection member may be disposed within a head portion of the vertebral anchors. At least a portion of the connection member may be a flexible member, such as a flexible cord, configured for tensioning between at least two vertebral anchors for providing a desired amount of tension to apply a correctional force to the spinal column. A spring member, or other tensioning member, may maintain the tension of the connection member.

Abstract: An anchor device for use in sacroiliac joint stabilization comprises a housing having a bore, one or more apertures, and a threaded outer surface, one or more engagement members at least partially disposed in the housing, where at least one of the one or more engagement members is movable between a retracted position and an extended position such that, when the at least one of the one or more engagement members is in the extended position, the at least one of the one or more engagement members extends through at least one of the one or more apertures, and where, when the at least one of the one or more engagement members is in the extended position, the at least one of the one or more engagement members is configured to engage a cortical wall of a sacrum bone.

Abstract: Devices for retracting tissue during a minimally-invasive, posterior spinal fusion procedure include a blade positionable along a passageway device connected to a connecting element implanted in a vertebra of the spine, such that the blade covers at least a portion of a longitudinal opening of the passageway device. The blade may be coupled to the passageway device by receiving the passageway device with a receiving portion. Systems for displacing the vertebrae of the spine include first and second extenders, the distal ends of each of which are configured to engage the connecting elements. Each extender may include a shaft configured to be securely engaged within a cage of the respective connecting element. The devices and systems of the present invention may be used in connection with an interbody fusion technique performed through an opening extending between the passageway devices, and an intermediate retractor blade may provide additional tissue retraction.

Abstract: Featured is a vertebral body manipulation instrument or vertebral body manipulation device being configured and arranged to allow correction of vertebral translation. Such a vertebral body manipulation device embodies one or more identical modules that are configured as needed for correcting the deformity. Such a vertebral body manipulation device also is usable in combination with a plurality of vertebral anchors, such vertebral anchors being any such vertebral anchors as are known to those skilled in the art (e.g., conventional spinal pedicle screw instrumentation) or hereinafter developed so as to form a spinal implant system. Also featured are treatment methods utilizing such a vertebral body manipulation device.

Abstract: Provided is an intramedullary (IM) rod for bone fixation. The IM rod is configured to be placed in an intramedullary cavity of a center portion of a part of a fractured bone which is required to be fixed to another part of the fractured bone, and lengthily extends in a direction of the part of the fractured bone, wherein the IM rod includes a plurality of guide holes configured to guide fasteners which are inserted through the part of the fractured bone and fastened to the other part of the fractured bone, and the plurality of guide holes include a main hole and a pair of sub-holes provided at positions forming vertices of a triangle together with the main hole.

Abstract: A femoral intramedullary device is capable of treating a variety of femoral bone fractures. The device includes an intramedullary nail capable of antegrade or retrograde insertion into the femur and having a shank long enough to extend into the shaft of the long bone and reach the corresponding distal area or proximal area and sockets located intermediate the ends of the shank for receiving anchoring pins or screws extended transversely or radially from the shaft of the long bone. The intramedullary nail is placed in the intramedullary canal of a portion of the bone and the screws are fixed in the radial sockets or receivers at the level of the femoral neck to provide mechanical support across the bone. Transverse screws are placed through the transverse sockets to provide additional support and secure the nail within the femur.

Abstract: Bone plate template systems and methods determine a suitable bone plate implant from a plurality of bone plate implants. The systems and methods have a first bone plate implant having a first length, and a second bone plate implant having a second length that is less than the first length of the first bone plate implant. The systems and methods have a bone plate template having a shape and a length defined between a first end and a second end located opposite to the first end, wherein at least a portion of the shape of the bone plate template corresponds to at least portions of a shape of at least one of the first and second bone plate implants. The bone plate template has at least one removable segment located adjacent to the second end of the bone plate template, wherein a connecting section of the bone plate template has a width and connects the at least one removable segment to the first end of the bone plate template.

Abstract: A bone repair system and method for percutaneously fixing a first bone segment to a second bone segment, such as rib bone segments, in a body of a patient include drilling a first hole through the first bone segment and a second hole through the second bone segment, and feeding a first tether through the first hole and a second tether through the second hole, each tether having a proximal end and a distal end. The first and second tether distal ends are withdrawn from the body while the first and second tether proximal ends have not passed through the first and second bone segments, respectively. A reinforcing member, such as a bone plate, having first and second openings, is passed onto the first and second tether distal ends, and the reinforcing member is pulled into engagement with the first and second bone segments guided by the tethers.