Abstract: An articulating rod inserter is configured for use in delivering a fixation rod to an orthopedic fixation system through a cannula or tower. The articulating rod inserter is releasably coupled to a rod and can move the rod from a generally aligned configuration, wherein the longitudinal axes of the rod and rod inserter are generally aligned, to an angled configuration, wherein the longitudinal axis of the rod is at an angle to the longitudinal axis of the rod inserter. The rod is inserted into the patient through a first tower and then articulated to a second tower such that the rod extends between two or more fixation devices.

Abstract: A suture anchor and methods of use thereof are disclosed. The suture anchor comprises an anchor body having a slot formed in the body and a passage extending through the body in a first direction. The passage is sized to permit a suture to traverse the body through the passage. The suture anchor also has a shaft with a sharp portion, and the slot and the passage intersect within the anchor body. The shaft is movable relative to the anchor body within the slot from a first position in which the sharp portion and the passage do not intersect, to a second position in which the sharp portion and the passage intersect. The shaft can penetrate a suture or multiple suture strands to fix the suture or suture strands relative to the suture anchor.

Abstract: A percutaneous spinal cross link system for interconnecting a spinal fusion construct on one side of the longitudinal axis of the spine with a spinal fusion construct on the other side of the longitudinal axis may include a cross bar connected at each end by a respective connector to a respective spinal fusion rod of each of the spinal fusion constructs. The connector may include a rod receiving portion adapted to receive one of the spinal fusion rods and a cross bar receiving portion adapted to receive the cross bar in an orientation generally perpendicular to the spinal fusion rod. A cannula defined by two spaced apart blades may be connected to the connector for defining a minimally invasive pathway through body tissue for introduction of the cross bar to the connector. Other tools for use with the system are also disclosed.

Abstract: Systems, devices, and methods suitable for use with procedures performed at least partially percutaneously are provided. In some procedures, two or more access devices for providing access to adjacent surgical locations within a patient are used. Certain embodiments of the access device comprise an elongate body having a distal end with one or more cutouts. The cutouts on adjacent access devices are generally aligned with each other to permit passage of a portion of a fixation element from one access device to the other access device. A fastener with an elongated removable head may be delivered to the surgical site through the access device. After a distal end of the fastener is secured to the surgical site, a portion of the elongated housing is detached from the remainder of the fastener and removed from the patient.

Abstract: Spinal stabilization implant assemblies, as well as systems, instruments and methods are provided for implanting and stabilizing adjacent vertebra in connection with a surgical procedure, particularly a spinal surgery. The implant assemblies and instruments enable controlled spinal rod insertion and reduction, and controlled rotation or de-rotation of adjacent spinal bones for optimized compression to achieve enhanced sagittal balance in a treated spine.

Abstract: Methods of applying a locking cap to a bone anchor assembly. The bone anchor assembly includes a bone anchor and an elongate rod. The bone anchor includes a body that defines a channel and has a tissue retractor coupled thereto that defines a partial pathway to the channel.

Abstract: A surgical instrument comprises a first member defining a cavity configured for disposal of a plurality of implants and including a distal portion that retains the implants with the first member. An element is configured to urge the implants in a first, release direction and the first member having at least one tab movable to prevent movement of at least one of the implants in a second direction. A second member is engageable with the at least one tab. Systems, spinal implants and methods are disclosed.

Abstract: Methods and devices are provided for anchoring a ligament or tendon to bone. In one embodiment, a surgical implant is provided having a sheath and an expander that is received within the sheath. Various delivery tools, including a sheath inserter and a driver, are also provided. In use, the sheath inserter can be used to position a tendon within a prepared bone hole, and it can be used to deliver the sheath with a guidewire coupled thereto into the bone hole. The driver can be provided for delivering the expander into the sheath. A loader can optionally be used to load the driver and expander onto the guidewire coupled to the implanted sheath.

Abstract: Methods and devices are provided for anchoring a ligament or tendon to bone. In one embodiment, a biceps tenodesis system is provided and includes a sheath inserter tool, an expandable sheath configured to couple to the sheath inserter tool, an expander inserter tool, and an expander configured to couple to the expander inserter tool. The sheath inserter tool is configured to advance the expandable sheath, with a tendon disposed therearound, into a bone hole, and the expander inserter tool is configured to advance the expander through an outer shaft of the sheath inserter tool and to drive the expander into the sheath. The expander is configured to be received within a lumen extending at least partially through the expandable sheath to thereby expand the sheath. In this way, the system delivers the tendon or ligament into the bone hole and locks the sheath and tendon within the bone hole.

Abstract: Methods, systems, and devices are provided for the alignment of implants or fastener members. For example, a surgical driver device is provided that has a driver head with a sidewall, a bore extending into a distal end of the driver head that is configured to receive an implant therein, and an alignment post that is disposed within the bore and extends distally beyond a distal opening of the bore. A retention member is disposed along a perimeter of the driver head and is configured to provide an interference fit between the driver head and an implant. A surgical caddie is also provided that has a housing, a plurality of implants on a mounting station, and a removal post that external threads that are matable with internal threads on each of the plurality of implants.

Abstract: An example implant delivery system is disclosed. The example implant delivery system includes a delivery shaft including a proximal portion, a distal portion and a lumen extending therebetween. The delivery system also includes a frame detachably coupled to the distal portion of the delivery shaft and a tack member coupled to the frame.

Abstract: A surgical tool adaptor includes a distal interface member and a handle. The distal interface member includes a connecting element for connecting to a surgical tool. A K-wire connector is disposed in a central passageway for receiving therethrough a K-wire. The K-wire connector includes a locking element for locking the K-wire. A clutch mechanism is operatively connected to the distal interface member and to the K-wire connector, wherein in a first orientation of the clutch mechanism, the distal interface member and the K-wire connector move together, and in a second orientation of the clutch mechanism, the distal interface member is declutched from the K-wire connector, so that in the first orientation movement of the handle moves the distal interface member and the K-wire connector together, and in the second orientation the distal interface member and the K-wire connector move independently of each other.

Abstract: A medical assembly and methods for endovascularly implanting a valve in the heart having a valve and an anchor assembly for positioning and restraining the valve. An anchor delivery system introduces and implants the anchor into the implantation site and a valve delivery system introduces and seals the valve at the deployment site. The present invention also relates to methods of implantation of the medical assembly and the valve.

Abstract: A medical assembly implanting an atrial sealing skirt in the heart at an atrial sealing skirt deployment site and related methods of implantation and delivery. An anchor is endovascularly introduced into the heart and implanted to a cardiac wall with an anchor delivery system and delivery cable. A second delivery system introduces a tether which coupled to the implanted anchor and an atrial sealing skirt. The atrial sealing skirt includes a top brim which is positioned to conform to the atrial floor at the deployment site. The sealing skirt may be integrated with a valve or serve as a receptacle.

Abstract: The present invention includes a device for engaging surgical tethers used in surgical repair, allowing for near full load application to the tether without failure at the site of restraint in the holding mechanism, with economical construction, compact size, and manageable complexity, without sharp edges that will cut the polymer fibers, and without requiring expensive polishing. The holding mechanisms comprise a tether, an orifice sheath, and a restraint element. The tether forms a bight projecting from the orifice sheath, the direction of projection being opposite to the direction of functional pull on the tether, where the bight is formed from a continuous tether or from coupled tether ends, and the restraint element is a fusiform structure positioned under the bight of the tether and over an orifice in the orifice sheath.

Abstract: A surgical tool of a surgical torque-transferring instrument includes a distal engagement segment or tool head which is adjoined by a tool shaft whose proximal end portion is prepared for a torque-transferring insertion into a tool mounting of the instrument. The proximal end portion is subdivided at least in a functional section for torque transmission and a functional section for axial locking which is axially spaced from the functional section for torque transmission. The functional section for axial locking, with respect to its geometry, includes parameters which are intended to be changed and cooperate according to the key/keyhole principle only with one tool mounting including corresponding geometrical mating parameters for a correct mounting of the tool.

Abstract: An apparatus includes a housing, an actuator, and a plurality of fasteners. The apparatus is for closing two sides of an incision or cut in skin tissue. The actuator moves into and out of the housing. The plurality of the fasteners are within the housing, and the apparatus is operable to deliver one fastener at a time into each of the two sides of the incision or cut.

Abstract: Methods and devices are disclosed for treating the facet joint. An implant for treating the facet joint is provided comprising a fixation plate having an access surface and a bone facing surface, a spacer configured to be inserted into the facet joint, and at least one hinge between the spacer and the bone facing surface of the fixation plate. A method for treating a facet joint comprising a superior articular process and an inferior articular process is provided comprising the steps of implanting a spacer between the superior articular process and the inferior articular process, positioning a fixation plate over the facet joint, and securing the fixation plate to at least one of the superior articular process and the inferior articular process. Another method comprises the steps of providing an implant comprising a fixation plate having an access surface and a bone facing surface, a spacer, and at least one hinge between the spacer and the bone facing surface of the fixation plate.

Abstract: Various bone anchor assemblies and methods are provided for anchoring tissue to bone. In one embodiment, an anchor assembly for anchoring a tendon to bone is provided and includes a substantially cylindrical sheath having bone-engaging surface features formed on an external surface thereof, and having an inner lumen formed therein and extending from an open proximal end to a substantially closed distal. The substantially closed distal end includes at least one tendon anchoring feature extending distally therefrom and configured to facilitate anchoring of a tendon to bone. The anchor assembly further includes an expander having a generally elongate cylindrical configuration and being sized and shaped to be received within the inner lumen of the sheath.

Abstract: Some embodiments described herein provide an improved tendon anchoring device and method for securing a muscle tendon to a bone. In particular, implementations described herein, the devices and methods are useful for anchoring a tendon to a bone in a patient's arm, including for example, anchoring a bicep tendon to bore formed in the targeted bone of the arm.

Abstract: An ankle implant for use in ankle arthroplasty in total ankle replacement is provided. The implant includes an upper prosthesis anchored to the tibia and a lower prosthesis anchored to the talus. The lower prosthesis is operable associated with the upper prosthesis. The implant also includes a stem which is rigidly removably connected to the second member. The stem includes a portion for attachment to the calcaneous. The stem is be adapted to be in a first position in the calcaneous when the stem is in a first relative position with respect to the lower prosthesis, and to provide for a second position in the calcaneous when the stem is in a second relative position with respect to the lower prosthesis.

Abstract: A laminar fixation system includes an implant and a implant installation tool for use with laminar fixation tape for retaining a spine rod relative to a vertebra of the spine. The implant has a spine rod locking portion, a laminar fixation tape channel, and a laminar fixation tape locking portion. The implant installation tool has a laminar fixation tape locking actuator for manipulating the laminar tape locking portion of the implant, and a laminar fixation tape tensioning sub-assembly for tensioning laminar fixation tape received in the implant. The laminar fixation tape locking actuator and the laminar fixation tape tensioning sub-assembly of the installation tool each operates independent of each other. Attachment of the implant to a spine rod via the spine rod locking portion of the implant is independent of laminar fixation tape tensioning and laminar tape fixation to the implant.

Abstract: An instrument includes a shaft and a mating element that extends from the shaft. The mating element is configured to engage a mating element of a bone fastener to move a receiver of the bone fastener relative to a bone anchor of the bone fastener. Implants, systems, constructs, instruments and methods are disclosed.

Abstract: A surgical instrument includes an actuator. A first member is connected with the actuator and is configured to engage a bone fastener that defines a first implant cavity and a second implant cavity. A second member is connected with the actuator and includes an implant engaging surface having a first portion movable along the first implant cavity and a second portion movable along the second implant cavity. Systems, spinal constructs, implants and methods are disclosed.

Abstract: Methods and devices are provided for anchoring a ligament or tendon to bone. In one embodiment, a surgical implant is provided having a sheath and an expander that is received within the sheath. Various delivery tools, including a sheath inserter and a driver, are also provided. In use, the sheath inserter can be used to position a tendon within a prepared bone hole, and it can be used to deliver the sheath with a guidewire coupled thereto into the bone hole. The driver can be provided for delivering the expander into the sheath. A loader can optionally be used to load the driver and expander onto the guidewire coupled to the implanted sheath.

Abstract: In one embodiment, a bone-plate placement tool guides a bone plate against an outer surface of a bone so that the bone plate can be fastened to an intramedullary nail received in a medullary canal of the bone. The tool includes a guide shaft and a plate holder. The shaft defines a bore extending therethrough along an axis. The plate holder couples to a bone plate, and is coupled to the guide shaft such that the plate holder angulates relative to the axis along a range of angles. The bore of the shaft and a bore of the plate holder combine to define a passageway that extends through the tool as the plate holder angulates relative to the axis along the range of angles so as to guide at least one of a drill bit and a bone anchor through the tool and into an aperture in the bone plate.

Abstract: An instrument for guiding a rod into a receiving area of an implant includes a coupling unit for coupling the instrument to the implant, a rod provided with an outer thread that can be positioned axially relative to the coupling unit, and at least one inner threaded segment arranged in an axially fixed manner relative to the coupling unit that can be brought into engagement or out of engagement with the outer thread of the threaded rod. The threaded rod has a stop, and the instrument has a locking element which is arranged in an axially fixed manner relative to the coupling unit for interacting with the stop. The locking element can be positioned in a radial direction relative to the threaded rod and is pretensioned in the direction of the threaded rod to engage with the stop by a pretensioning element which applies a radial force.

Abstract: An illustrative example suture securing assembly includes an inserter, a rigid member and a second member. The inserter includes a distal end, a proximal end, and a longitudinal axis between the distal end and the proximal end. The inserter includes a handle near the proximal end and a rotatable portion near the handle. The rigid member includes an eyelet oriented to thread suture across the longitudinal axis. The rigid member is situated near the distal end of the inserter. The rigid member is configured to be placed in bone. The second member is situated near the distal end of the inserter and is configured to be rotated by the rotatable portion of the inserter to rotationally advance the second member in a distal direction toward the eyelet into a suture securing position where the second member holds suture in place.

Abstract: A method for securing soft tissue to bone which does not require the surgeon to tie suture knots to secure the tissue to the bone. Suture is passed through the graft at desired points. A cannulated plug or screw is pre-loaded onto the distal end of a driver provided with an eyelet implant at its distal end. Suture attached to the graft is passed through the eyelet of the implant located at the distal end of the driver. The distal end of the driver together with the eyelet implant is inserted into the bone. Tension is applied to the suture to position the graft at the desired location relative to the bone. The screw or plug is advanced into the pilot hole by turning the interference screw or tapping the plug until the cannulated screw or plug securely engages and locks in the eyelet implant, so that the cannulated plug or screw with the engaged eyelet implant is flush with the bone.

Abstract: The invention relates to a medical instrumentation, comprising a hand-held, integrated, medical navigation system which comprises an optical detection unit having a camera, a data processing unit and an optical display unit, the data processing unit being coupled to the detection unit and the display unit, it being possible for location and/or orientation data of a medical marking device which is detectable with the detection unit to be processed by the data processing unit and information relating thereto to be represented on the display unit, the instrumentation comprising an illumination unit with which light is emittable in the direction of the marking device detectable with the detection unit.

Abstract: The invention relates to an extension device (2) for a bone anchor (4), in particular for a pedicle screw having an axial longitudinal direction (16), a circumferential direction (18) concentric thereto and a radial direction (20), wherein the extension device (2) is extended in the axial longitudinal direction (16) and can be detachably fixed to the head (8) of the bone anchor (4), wherein the extension device (2) comprises two shell parts (22) that are separate from each other and extended in the longitudinal direction 16, characterized in that, the extension device further comprises a sleeve-like housing part (60) that can be slid in the axial longitudinal direction (16) onto the two shell parts (22) which are separated from each other and detachably fixed to the head of the bone anchor and, in the applied state, limits and defines a tunnel-like access (106) to the bone anchor (4) that extends in the axial direction (16).

Abstract: A surgical instrument for separating an introducer sheath from a device connected to the introducer sheath is disclosed. In embodiments, the surgical instrument includes an extension extending in a longitudinal direction; a pin; and a separator connecting the extension and the pin.

Abstract: Instruments are provided for shifting elongate members, such as spinal rods, with respect to coupling members of spinal fixation systems. The instruments include a low friction drive mechanism having one or more rolling elements that ride along a helical groove or track in order to transform rotational movement of a drive member into linear shifting of a reducer member that shifts the elongate member. A one-way locking mechanism may be provided to selectively prevent unwanted counter-rotation of the low friction drive mechanism. The one-way locking mechanism may include annular ratchet teeth arranged on the exterior of the drive member and a ratchet pawl located adjacent to the teeth and selectively engageable therewith.

Abstract: Implantable tensile load-bearing grafts having synthetic components stitched through biological components are disclosed. The synthetic components can be biodegradable and/or non-biodegradable and of differing tensile strengths from each other and the biological component. Methods of making the grafts are also disclosed.

Abstract: Implementations described and claimed herein provide a bone anchor deployment device. In one implementation, the bone anchor deployment device includes a flexible shaft adapted to bend along a deployment trajectory. A socket at the distal end of the flexible shaft is adapted to retain a bone anchor in a non-coaxial position. The bone anchor deployment device further includes a guide shaft having a lumen and a distal tip and an elongated tube extending through at least a portion of the guide shaft lumen and protruding from the distal tip of the guide shaft. A guide passage extends through a lumen of the elongated tube, and a channel is formed from a surface at a distal end of the guide passage. The channel is oriented at an angle relative to the guide passage and is adapted to cause the flexible shaft to bend.

Abstract: A system for fixating a dysfunctional sacroiliac joint for SI joint fusion, the system including a sacroiliac joint implant and a delivery tool configured for approaching a sacroiliac joint. The system may include an implant having a porous 3D matrix structure and may be manufactured by laser or electron beam additive manufacturing. The delivery tool may include a radiolucent material. The SI fusion system may further include custom sacroiliac joint implants, anchors, alignment tools or targeting arms manufactured for a particular patient. Pre-surgical imaging studies, including 3D rendering, and their interpretation may assist in planning desired trajectories, anchor dimensions and implant dimensions and may provide details specific to the manufacture of particular sacroiliac joint tools or implants and their implantation into the sacroiliac joint. The system may be configured for use with surgical robots and may include an integrated nerve monitoring and stimulation system.

Abstract: A method for interosseous ligament reconstruction (e.g., of a scapholunate or lunotriquetral ligament) includes drilling holes through both of the bones to allow for a graft to be placed on the volar and dorsal aspects of the bones, replicating the normal anatomic structure of the interosseous ligament, while requiring only an incision on the dorsal side of the wrist. The method includes using a drill guide that directs the drill to place a drill hole from dorsal to volar (front to back) in the bone, while making sure the drilled hole is within the joint on the volar side. The drill guide includes a hollow guide tube to advance a drill through, the hollow tube movably coupled to a shaft of the drill guide with a distal end that generally aligns with the distal end of the hollow tube.

Abstract: A device may include an outer sleeve with a hollow interior, and an inner sleeve with a hollow interior to couple axially and slidingly. The outer sleeve may include an outer central body, an outer proximal end part and an outer distal end part integrally connected to one another, and an outer channel extending along the entire outer proximal end part and along a substantial portion of the outer central body. The inner sleeve may include an inner central body, an inner proximal end part and an inner distal end part integrally connected to one another, and an inner channel extending along the entire inner proximal end part and along a substantial part of the inner central body. The inner sleeve may include, in the inner proximal end of the inner sleeve, a lateral engagement element, and an axial engagement element for releasably engaging a surgical screw.

Abstract: A fixation device. At least one example embodiment is a bone anchor comprising: a proximal head; a bollard coupled to the proximal head; a first barb coupled to the bollard, the first barb extends outward a first distance measured perpendicularly from an anchor central axis, the first distance greater than half the transverse dimension of the bollard, and the first barb extends outward at a first radial from the anchor central axis; and a second barb coupled to the first barb, the second barb extends outward a second distance measured perpendicularly from the anchor central axis, the second distance greater than half the transverse dimension of the bollard, and the second barb extends outward at a second radial from the anchor central axis, the second radial at a second rotational orientation at least 36 angular degrees from the first radial.

Abstract: A tool set for implanting a rod in a human spine in conjunction with bone screws includes a pair of end guide tools that receive opposite ends of the rod in channels and under manipulation by a surgeon facilitate transport of the rod toward the bone screws attached to the guide tools. Each end guide tool includes a laterally extending, rigid, rod holding structure located near a bottom surface thereof. Intermediate guide tools having pass-through slots are utilized to guide the rod to the bone screws at intermediate locations. For bone screw implantation, the end guide tools and intermediate guide tools are assembled with a driver. The driver is coaxial with the respective guide tool and rotatingly mateable thereto. The driver includes a stem and a nut-type fastener, the stem receivable in the guide tool. The fastener allows for rotation of the bone screw without rotating the attached guide tool.

Abstract: Novel bone screw and plate assemblies including locking confirmation mechanisms are provided. In certain cases, a locking confirmation mechanism is operably attached to the plate, and comprises a toggling arm having an upper portion, a mid-portion and a lower portion. When a bone screw is positioned in a plate in an unlocked configuration, the locking confirmation mechanism assumes a first position. When the bone screw is positioned in the plate in a locked configuration, this causes the locking confirmation mechanism to pivot and assume a second position. The locking confirmation mechanism thus provides a convenient visual and/or tactile means to assess when the screw is in a locked configuration.

Abstract: In one embodiment, a medical device includes a tissue anchor has a first portion and a second portion. The tissue anchor is configured to be placed within bodily tissue of a patient. The first portion of the tissue anchor includes an extension member configured to engage the bodily tissue to help retain the tissue anchor within the bodily tissue. The first portion has an inner surface and defines a cavity. The second portion of the tissue anchor has a helical ridge. The helical ridge is configured to engage the inner surface of the first portion of the tissue anchor to movably couple the second portion of the tissue anchor to the first portion of the tissue anchor.

Abstract: A reduction sleeve for facilitating insertion of a spinal rod into a rod-receiving channel formed in a bone fixation element. The reduction sleeve may include a through-bore sized and configured to receive the bone fixation element and a substantially transverse channel sized and configured to receive the spinal rod. The channel being substantially aligned with the rod-receiving channel formed in the bone fixation element so that, once the bone fixation element has been inserted into the reduction sleeve, the spinal rod can pass through the aligned channels. The reduction sleeve may also include at least one break-off point or region for facilitating breaking and removal of the reduction sleeve once the spinal rod has been clamped into the rod-receiving channel of the bone fixation element.

Abstract: A knotless suture anchoring system includes an outer anchor having a central channel and a distal tip adapted to penetrate tissue. An inner anchor is positionable in the central channel of the outer anchor and a locking feature on one or both of the inner and outer anchors retains the inner anchor within the central channel. A continuous length of suture is coupled with the inner and outer suture anchors and has a free end. At least one of the inner and the outer anchors also has a cinching mechanism that allows the suture to be tensioned by passage of the suture through the cinching mechanism in a first direction while movement of the suture through the cinching mechanism in a second direction opposite the first direction is constrained.

Abstract: The self-locking screwdriver includes a guide tube inside which a clamping rod is guided and rotatably driven, one end of which is provided with a cavity which allows the rotational drive and tightening of an anchoring screw, ensuring the immobilization of an orthopedic implant against an osseous body of an individual, the screwdriver including, on the one hand, between The guide tube and the clamping rod, a blocking system cooperating with the guide tube in order to prevent the latter from being loosened from the orthopedic implant when the anchoring screw is tightened and, on the other hand, on the outer periphery of the guide tube, a gripping wheel for locking and/or unlocking the blocking system and the rotational drive of the guide tube.

Abstract: A bone fastener includes a proximal portion including an inner surface defining an implant cavity. A first member is configured for disposal with the proximal portion and includes a wall defining a cavity. A second member is configured for disposal with the cavity. A distal portion includes a first end disposed within the members and a second end configured to penetrate tissue. The proximal portion overlaps the second member to limit movement of the first end of the distal portion. Systems and methods are disclosed.

Abstract: A simplified placement system and method for a tissue graft anchor by which a surgeon may introduce one or more sutures into a socket in a boney tissue, apply a precise amount of tension to the sutures to advance a soft tissue graft to a desired location, and then advance the anchor into the socket, preferably while maintaining the requisite pre-determined suture tension and without introducing spin to the suture is disclosed. Alternate embodiments of the anchor placement system and method of the present invention may forego tensioned sutures in favor of direct engagement with the soft tissue graft, whereby an end or a portion of the graft is trapped between an outer surface of the anchor and the boney surface of the wall of the socket such that friction force between the inserted portions of graft and socket maintains the position of graft relative to socket and bone. In either case, particularly preferred embodiments allow for the one-handed operation.

Abstract: The present application discloses embodiments related to an implant and a method of forming an implant configured to treat a fractured bone. The implant can include a body having a proximal end, a distal end, and an outer surface extending from the proximal end to the distal end, wherein the body defines a central axis extending from the proximal end to the distal end; and a high tensile strand positioned adjacent the body such that at least a portion of the strand extends at least partially along the outer surface of the body in a direction substantially parallel with the central axis, and wherein the strand is loaded with an active agent.

Abstract: A maxillomandibular fixation (MMF) device having an arch bar with a plurality of spaced tabs and gaps, and further having apertured mounting plate members mounted onto the arch bar, each mounting plate member having a slot to receive a tab on the arch bar, whereby the mounting plate members may be repositioned laterally along the arch bar from one tab to another prior to affixing the MMF device to the maxilla or mandible of a patient in order to position the mounting plate members at locations where the underlying tooth root will not be damaged by insertion of a bone screw.

Abstract: Methods and apparatus are disclosed for performing spinal reconstructive surgery, including measuring spinal length in the Y-axis at the middle column, measuring intervertebral spacing in the Y-axis at the middle column, measuring intervertebral tension applied to the posterior longitudinal ligament, establishing the height of intervertebral spacers along the Y-axis at the middle column based on one or more of such measurements, measuring intervertebral rotation around the Y-axis, and measuring flexion-extension or anterior-posterior rotation around the X-axis.