Abstract: The present invention includes a surgically implantable device, system, and method of use thereof for the internal compression or distraction of, for example, bone fractures, fusions, and osteotomies. More specifically, the surgical device comprises a bridge with one or more adjustable anti-reversing portions. The adjustable anti-reversing portion(s) may be located in a symmetrical or asymmetrical manner on the bridge between the device's legs. The adjustable anti-reversing portion(s) allow for stronger compression of the bone at a known amount of compression. The adjustable anti-reversing portion(s) can also maintain the device's legs in closer proximity to one another for greater compression or maintain the device's legs apart from one another for distraction. The surgical device can also comprise cannulated or grooved legs. A system and method of use is also described.

Abstract: A spinal fixation assembly and capless multi-axial screw system and method are shown. The assembly comprises a receiver having a rotary lock which in one embodiment includes a plurality of channels which urge and lock the elongated member to the screw using a bayonet type connection.

Abstract: The present invention provides a suture anchor capable of securing a suture to a body tissue.

Abstract: Spinal surgical systems, instruments and methods include a surgical instrument with a first member mountable to a first vertebra and a second member mountable to a second vertebra. The first and second members are coupled to one another with a coupling mechanism that allows translation of the first and second members relative to another along a predetermined path. The coupling mechanism also provides a pivot axis about which the first and second members are manipulated relative to one another to deliver forces to the first and second vertebrae.

Abstract: An intervertebral implant includes a body for insertion between adjacent vertebrae, and one or more anchors extending from the body for securing the body between the vertebrae. A linear motion control mechanism is mounted in the body and operable to limit linear translation of the anchor(s) relative to the body. Also, a pivot control mechanism in the body operates to limit pivot motion of the anchor(s) relative to the body. The linear and pivot control mechanisms are configured in various arrangements and embodiments exhibiting adjustable dynamic settings, allowing a single implant to provide various types of dynamic fixation with ranges of motion that permit loads to transfer to graft material contained in the disk space.

Abstract: A medical implant system is described for inhibiting infection associated with a joint prosthesis implant. An inventive system includes an implant body made of a biocompatible material which has a metal component disposed on an external surface of the implant body. A current is allowed to flow to the metal component, stimulating release of metal ions toxic to microbes, such as bacteria, protozoa, fungi, and viruses. One detailed system is completely surgically implantable in the patient such that no part of the system is external to the patient while the system is in use. In addition, externally controlled devices are provided which allow for modulation of implanted components.

Abstract: An apparatus includes a first elongate member and a second elongate member. The first elongate member has a proximal end portion that includes a threaded portion, and a distal end portion that includes a retention portion. The retention portion of the first elongate member is configured to deform when moved from a first configuration to a second configuration. At least a central portion of the second elongate member is disposed within the first elongate member. The second elongate member has a distal end portion that includes an actuation portion configured to deform the retention portion of the first elongate member from the first configuration to the second configuration.

Abstract: An apparatus and method for fixing a selected graft relative to a selected anatomical portion. An anchor may be provided that may be interconnected with a selected graft portion that is operable to pass through a selected bore and then moved into an operable position to engage a selected portion of the bore to substantially eliminate the possibility of the graft moving in an unselected direction through the bore.

Abstract: A repair system for a compromised or herniated spine disc is provided. The repair system includes a spine disc patch to cover the herniation, and hooks, fasteners or the like to attach the spine disc patch to the vertebra surrounding the compromised disc. The repair system also includes an application tool to introduce and deploy the spine disc patch and spine disc patch fasteners to and on the disc herniation site. The spine disc patch is composed of a mesh, screen or the like of a biocompatible material with a perimeter, edge or side portion formed of a resilient biocompatible material. The mesh is preferably, but not necessarily, formed of a flexible but non-resilient biocompatible material. The perimeter is preferably, but not necessarily, formed of a flexible, resilient biocompatible material.

Abstract: A tape made of polyester fibers is disclosed which, though a flexible tape, is not easily elongated when it is pulled. The tape is a tape which is produced by braiding polyester fibers into a tape and then subjecting it to drawing, and whose maximum Young's modulus measured on a stress-elongation curve produced as it is pulled until its elongation reaches 5% of its initial length is not less than 2 GPa.

Abstract: A tulip assembly configured to be coupled to a head of a bone fixation device includes at least one inner member configured to fix the tulip assembly to the head of a bone fixation device, and an outer member including at least one engagement surface configured to selectively fix a rod in the tulip assembly via rotation of the outer member, wherein the fixation of the tulip assembly to the head of the bone fixation device is independent of the fixation of a rod in the tulip assembly.

Abstract: A surgical anchor device for the repair of a torn ligament or tendon, primarily the anterior cruciate ligament in the knee, is used to affix the ligament within a femoral bone tunnel in the distal portion of the femur from the intra-articular surface, the device providing a pulley for a suture, wherein a free end of the suture may be pulled away from the device to draw the suture attached to the ligament graft within the femoral bone tunnel securing the ligament graft within the bone tunnel. Installation of the device is provided by insertion of the device through a tibial hole, through the femoral tunnel out of the lateral femoral cortex, pulling the attached sutures simultaneously to flatten the device against the lateral femoral cortex, attaching one end of the suture to the ligament graft and pulling the other end of the suture until the graft is situated properly within the femoral bone tunnel and tying the free end of the suture to retain the graft within the femoral bone tunnel.

Abstract: Systems and methods for positioning a connecting element adjacent an anatomical structure in minimally-invasive surgical procedures, including an electronic guidance system associated with the connecting element and at least one receiving portion of a tissue anchor that receives the connecting element in the patient. The electronic guidance system includes a processor subsystem to receive signals from the guidance system and provide relative positional data between the connecting element and the at least one receiving portion to aid the surgeon in guiding the connecting element to the receiving portion. In one embodiment, the systems and methods are used in association with positioning a connecting element adjacent the spinal column in minimally-invasive spinal stabilization procedures.

Abstract: A knotless suture anchor for reattachment of tissue to bone features a barbed body having a Y-shaped slot formed distally for capturing a length of suture. The suture is passed through the tissue to be reattached, and a simple knot formed in the suture is captured in the slot on the suture anchor. The anchor is installed with the captured suture into a pre-formed pilot hole to draw the tissue to the bone.

Abstract: In one aspect of the invention, a cross-pin includes a distal portion having an axis, a distal end, and a proximal end. A proximal cylindrical portion includes a threaded exterior surface. A junction may be interposed between the distal and proximal portions to enable the proximal portion to rotate relative to the distal portion. In another aspect of the invention, a graft retaining system for retaining a graft in a bone tunnel includes a graft block having a proximal end and a distal end, and sized to fit within the bone tunnel. A cross pin transverse to the bone tunnel attaches the graft block adjacent the tunnel. An intermediate connector is attached to the graft block at a point distal to the cross pin and connects the graft to the graft block so as to apply compressive forces to the graft block.

Abstract: A bone anchor device for attaching connective tissue to bone comprises a disk adapted for insertion into a portion of bone to which the connective tissue is to be attached. The disk is movable between a bent orientation for presenting a smaller cross-section and an expanded orientation for presenting a larger cross-section. The bent orientation is utilized for inserting the disk through a small hole into a region of cancellous bone beneath the cortical bone layer, after which the disk is actuated to its expanded orientation so that it will be permanently anchored in the cancellous bone, as it will be too large to return proximally through the hole in the cortical bone layer. Two embodiments are disclosed. In a first embodiment, the disk is initially formed in the expanded orientation, of spring steel. In a second embodiment, the disk is initially formed in the bent orientation, and spring steel is not required.

Abstract: A suture fixation apparatus having a first body portion having a bone engaging feature to fixedly engage a bony tissue and a second body portion defining an eyelet for receipt of a suture. The second body portion is rotatable with respect to the first body portion. Rotating the second body portion causes the suture to form a twist to frictionally secure the suture.

Abstract: An implant is provided for fixing neighboring bone plates of the cranial bone in a simple and reliable manner. The implant comprises an outer bearing element for covering a spacing gap between the bone plates, which sits on outer surfaces of the bone plates. The outer bearing element has a first pair of outer openings and a first pair of inner openings. An inner bearing element is provided for covering the spacing gap between the bone plates, which sits on inner surfaces of the bone plates. The inner bearing element has a second pair of outer openings and a second pair of inner openings. A thread-like tensioning element is provided which is threaded through the openings of the outer and inner bearing elements in a displaceable manner, such that, when tensioned, the tensioning element draws the inner bearing element and the outer bearing element together.

Abstract: The longitudinal implant is fastened to bones on either side of a damaged area through a connecting device. Said implant is comprised of a filament or fiber composite material and said connecting device is made of a material harder than said longitudinal implant. The longitudinal implant is preferably made of a carbon filament composite material, wherein the filament are encapsulated in a polymer matrix.

Abstract: An orthopaedic implant system includes an orthopaedic implant implantable at a selected location within a corporeal body. The implant includes a first structural material and a second structural material. The first structural material is non-resorbable relative to the corporeal body and is different relative to the second structural material. The implant is an internal fixation device.

Abstract: A polyaxial bone screw having a bone implantable shank, a head and a retaining ring. The retaining ring includes an outer partial hemispherical surface and an inner bore with radially extending channels and partial capture recesses. The shank includes a bone implantable body with an external helical wound thread and an upwardly extending capture structure. The capture structure includes at least one spline which extends radially outward and has a wedged surface that faces radially outward therefrom. The capture structure operably passes through a central bore of the retaining ring while the spline passes through a suitably shaped channel so that the spline becomes positioned above the head at which time the shank is rotated appropriately and the shank is drawn back downwardly so that the spline engages and seats in the capture recess.

Abstract: A bone anchor includes a screw portion configured to penetrate a bone. The screw portion includes a retention thread extending at least part of a length of the screw portion and a tip at a first end of the screw portion. The bone anchor includes a protrusion adjacent a second end of the screw portion. The second end is opposite the first end of the screw portion. The protrusion comprises a plurality of external sides forming a shape and a rounded interior surface enclosing a protrusion recess. The rounded interior surface includes a recess thread configured to retain a component at least partially in the protrusion recess. The protrusion has a maximum width that is less than a maximum diameter of the screw portion such that a shoulder is formed where the protrusion meets the second end of the screw portion.

Abstract: An implantation device for fixating a bone has a main body. The main body has a peripheral region and comprises a polymeric material. The peripheral region comprises the polymeric material and a plasticizer. In particular, the peripheral region may be adapted to be fixed to a bone. A method for producing the implantation device includes the steps of forming an implantation device using polymer material, and dipping at least a portion of the implantation device into a plasticizer in such a way that a peripheral region of the implantation device is plasticized.

Abstract: A system and method for use in spinal surgery to alleviate a bulging/herniated disc. The method comprises inserting a first cannula into a vertebra, and inserting a first anchor into the first cannula through the vertebra and into a disc, the first anchor generating a magnetic field pointing in a first direction. The method further comprises inserting a second anchor through the first cannula and through the vertebra, the second anchor generating a magnetic field pointing in the first direction, the second anchor including a second cannula; and pulling the second cannula to anchor the second anchor into the vertebra. As the magnetic fields are in the same direction, the first anchor repels the second anchor thereby pushing a bulging disc back in place.

Abstract: The present disclosure relates to an anchor. The anchor includes an outer member including a body having an inner cavity, wherein the inner cavity includes a proximal portion configured for receipt of a delivery device and a distal portion having area of increased diameter. The anchor also includes an inner member coupled to the outer member, wherein the inner member includes a proximal portion having a projection configured for receipt in the area of increased diameter and a distal portion having a transverse through hole. A delivery device and method for tissue repair are also disclosed.

Abstract: A device for use in tissue repair procedures, a surgical tissue repair procedure, and a method of making the device. Specifically, the device is an assembly of a cannulated anchor member with a cord passed through it, and a stopper mounted to an end of the cord to prevent the cord from passing back through the anchor member.

Abstract: A suture anchor includes a placement portion frangably connected to an attachment portion. The attachment portion includes an outwardly projecting barb. During insertion of the suture anchor within a bore hole formed on a bone, the barb scores at least a portion of the bone bounding the bore hole. Once the suture anchor is disposed within the bore hole, a withdrawal force is applied to the suture anchor such that the attachment portion thereof rotates within the bore hole and disconnects from the placement portion. In an alternative embodiment, the suture anchor can be formed without the outwardly projecting barb.

Abstract: A repair kit for use in the repair of damaged cartilage present at or on the surface of a bone site in an animal or human, in which the damaged cartilage is removed from the site and a groove is formed about the site and into the bone prior to implantation of the repair kit. The repair kit includes: a pad of bio-compatible material shaped and dimensioned to occupy at least part of the site from which the damaged tissue has been removed. Elongate connecting portions are attached to the periphery of the pad in an array corresponding in shape to the groove. The connecting portions extend away from the general plane of the pad so as to be introduced into the groove and to be anchored therein. A retaining element is slidable depthwise of the groove to anchor at least some of the connecting portions in the groove and thereby locate and retain the pad in the part of the bone site.

Abstract: A spinal joint distraction system is disclosed and may include a driver assembly with a tubular shaft, a pair of implant holder arms, an implant distractor, an internal actuator, and a distractor knob, the system also including a delivery device with a tubular shaft, a receiving assembly, and a pair of forks, where the delivery device is adapted for slidable insertion of the driver assembly, the system also including an implant, a chisel, and an injector. Several embodiments of an implant are disclosed as well a method of placing an implant.

Abstract: A bone screw has a flexible shaft which prevents relative movements in the direction of tension, but permits smaller movements in all other directions. The bone screw is configured as a screw insertable into medullary cavities having a curved surface, where the screw adapts to the given contour.

Abstract: The forces exerted on a spinal implant by one or more coupling assemblies are controlled to facilitate the use of the implant in spinal stabilization and other procedures. The coupling assemblies are structured to distribute the forces exerted on the implant while engaging the implant to the coupling assembly and providing at least one of a rigid, semi-rigid or variable engagement of the coupling assembly with one or more anatomical structures of the spinal column.

Abstract: Systems for minimally invasive disc augmentation include an anulus augmentation component and a nucleus augmentation component. Both are suited for minimally invasive deployment. The nucleus augmentation component restores disc height and/or replaces missing nucleus pulposus. The anulus augmentation component shields weakened regions of the anulus fibrosis and/or resists escape of natural nucleus pulposus and/or the nucleus augmentation component. Methods and deployment devices are also disclosed. Methods of closing a defect in an anulus fibrosus of an intervertebral disc using a barrier are also provided.

Abstract: A device for use in tissue repair, a method of using the device in a surgical procedure and a method of making the device. The device is an assembly of a anchor with a cord passed through it, and a stopper to prevent the cord from passing back through the anchor.

Abstract: Aspects of the present disclosure include a bone plate and/or a bone plate system. The bone plate includes an elongate body, which body includes a distal portion and a proximal portion. The proximal portion includes at least one projection extending there from, which projection is configured for contacting a bone portion, e.g., a fractured bone portion, so as to aid in the reduction thereof. In some variations, the proximal portion includes a plurality of projections, e.g., reduction aids. Methods of using such a bone plate having reduction aids by itself, or in conjunction with a second bone plate, for the reduction, restoration and treatment of a bone fracture are also provided.

Abstract: A suture-loading system, method and apparatus for loading a suture onto a bone anchor, the system comprising: a bone anchor comprising a suture leg-anchoring structure and a plurality of body holes on the anchor; a suture comprising a standing end portion and a working end portion; a standing end trackway to guide the standing end portion of the suture through the suture leg-anchoring structure; and a working end trackway to guide the working end portion of the suture through the body holes in the anchor.

Abstract: An artificial ligament assembly for spinal stabilization includes an outer hollow elastic longitudinal member, a rigid inner member, a bone anchor mechanism, a bone anchor, and a buffered space. The artificial ligament assembly further includes a clamp that controls a torsional motion of the outer hollow elastic longitudinal member with respect to the bone anchor mechanism. The outer hollow elastic longitudinal member is at least as long as the inner rigid member. The rigid inner member is configured in a substantially same shape as the outer hollow elastic longitudinal member. The bone anchor mechanism is coupled to the outer hollow elastic longitudinal member. The bone anchor connector may further include an insert end. The bone anchor is coupled to the bone anchor mechanism. The buffered space allows any of a compression and an extension of the bone anchor mechanism inside the outer hollow elastic longitudinal member.

Abstract: A system and method for attaching soft tissue to a prosthetic implant can include a prosthetic component that defines a soft tissue attachment region having an attachment surface thereon. A first construct can be formed of porous metal and be removably coupled to the attachment surface. A second construct can be positioned outboard of the soft tissue. A fastener can be engaged to the second construct capturing the soft tissue against the first construct. The fastener can be coupled on a distal end to the first prosthetic component.

Abstract: This disclosure presents methods and devices for treating a tear, rent, incision, defect, aperture or delamination of the annulus fibrosus of an intervertebral disc. The methods and devices can employ fixation delivery apparatuses, fixation apparatuses, patch delivery tools and patches positioned, at least in part, in or on aspects of an intervertebral disc for treatment of the intervertebral disc or its components. In some aspects, these techniques include the use of this includes a fixation apparatus that includes at least one bone anchor connected to at least one disc anchor by a shortenable elongate member.

Abstract: An anchor is implantable into a bone in a patient's body and, when implanted, is resistant to toggling in the bone and to being pulled from the bone. The anchor includes a head end portion having a surface that extends transverse to a central axis of the anchor and is engagable with the bone. A plurality of helical spikes extend from the surface on the head end portion and are engagable with the bone. Each of the plurality of helical spikes has a helical central axis that forms a helix around the central axis of the anchor. Each of the plurality of helical spikes further has a circular cross-sectional configuration as viewed in a plane extending perpendicular to the helical central axis of each of the helical spikes and a distal end portion with a tip that penetrates the bone as the head end portion is rotated relative to the bone.

Abstract: A fixation system for a bone conduction device is disclosed. An abutment is coupled to a bone anchor such that vibrations applied to the abutment pass into the bone anchor. The abutment defines a conduction path to the bone anchor such that vibrations applied to the abutment are transferred to the bone anchor. The abutment comprises a plurality of shearing elements disposed adjacent the bone anchor, wherein the shearing elements form part of the conduction path. The fixation system also comprises a vibratory coupler extending from the bone conduction device, comprising a second conduction surface and a magnet, wherein the magnet attracts to the abutment so as to couple the second conduction surface to the abutment, thereby enabling vibrations to pass through the conduction path. The shearing elements are configured to slide laterally in response to tangential forces incident upon the abutment.

Abstract: A fixation system for a bone conduction device is disclosed. The fixation system comprises an implantable anchor comprising a plurality of elements configured to be implanted in at least one of the one or more layers of tissue adjacent the skull of a recipient such that vibrations applied thereto are transferred to the skull. The fixation system further comprises a vibratory coupler, extending from the bone conduction device, comprising a conduction surface and a magnet, wherein when the conduction surface is adjacent the one or more layers, the magnet is attracted to the implantable anchor to retain the conduction surface adjacent the one or more layers, thereby enabling vibrations to pass from the bone conduction device to the skull.

Abstract: A fixation system for a bone conduction device is disclosed. An abutment is coupled to a bone anchor such that vibrations applied to the abutment pass into the bone anchor. The abutment defines a conduction path to the bone anchor such that vibrations applied to the abutment are transferred to the bone anchor. The abutment comprises a plurality of interlocking stacked plates disposed adjacent the bone anchor, wherein the plates form part of the conduction path. The fixation system also comprises a vibratory coupler extending from the bone conduction device, comprising a second conduction surface and a magnet, wherein the magnet attracts to the abutment so as to couple the second conduction surface to the abutment, thereby enabling vibrations to pass through the conduction path. The plates are configured to slide laterally in response to tangential forces incident upon the abutment.

Abstract: A stabilization rod engaging apparatus for implantation in a patient includes: a first pivot element including at least one first aperture, a first engagement element, and a first locking element; a second pivot element including at least one second aperture, a second engagement element, and a second locking element, wherein: the first and second apertures are sized, shaped and disposed in substantial axial alignment such that they are operable to receive the stabilization rod therethrough, and displacement of the first and second locking elements relative to one another urges the first and second apertures to misalign and thereby clamp the stabilization rod.

Abstract: A method for fabricating a device for repairing torn tissue or muscle such as the meniscus of the knee. The device includes a pair of anchoring members having a plurality of barb-like projections extending outwardly therefrom. The anchoring members are joined by a flexible linking member which connects the ends of the anchoring members opposite one another. Such a device can be fabricated by insert molding of the appropriate members together.

Abstract: A press-fit prosthesis for replacing a portion of a bone. The prosthesis can comprise a first side and a second side opposite the first side. The second side can be operable to engage the bone. The prosthesis can include at least one resorbable fixation member coupled to the second side such that the at least one resorbable fixation member does not extend through to the first side. The at least one resorbable fixation member can be coupled offset from a center of the second side. The at least one resorbable fixation member can substantially resist movement of the prosthesis relative to the bone. The at least one resorbable fixation member can resorb at a rate that enables bone in-growth to fixedly couple the prothesis to the bone.

Abstract: Minimal Invasive Spine Surgery (MISS) as a surgical approach is increasingly utilized because of the advantages it offers over conventional spine surgery. The smaller incision results in decreased tissue damage, less blood loss, decreased hospital stay & faster postoperative recovery. The drawbacks of MISS are the long learning curve of working through a smaller incision, longer length of surgery, & potential higher complication rate due to compromised visual field. These limitations can be overcome by more effectively using imaging and navigational devices. The pedicle device simplifies the hardest part of MISS instrumented fusion of conventional pedicle screw insertion by introducing a percutaneous temporary device to locate and create the channel for later conventional pedicle screw implantation using available imaging techniques.

Abstract: A device for attaching connective tissue to bone has a longitudinal axis and comprises an annular toggle member and a body member disposed distally of the toggle member, such that there is an axial space between the toggle member and the body member. The toggle member is movable between an undeployed position wherein the toggle member has a smaller profile in a direction transverse to the axis and a deployed position wherein the toggle member has a larger profile in the direction transverse to the axis. When installed in a desired procedural site, in suitable bone, suturing material extends axially through a center aperture in the annular toggle member, without being secured to or contacting the toggle member. This approach permits a suture attachment which lies entirely beneath the cortical bone surface, and which further permit the attachment of suture to the bone anchor without the necessity for tying knots, which is particularly arduous and technically demanding in the case of arthroscopic procedures.

Abstract: Disclosed herein are devices and methods for securing soft tissue to a rigid structure such as bone. Various directional anchors that allow for increasing the stability the attachment of soft tissue to bone are described. Also described is a delivery system for use with the directional anchors that allows for open surgical or arthroscopic application of one embodiment of the device. A method for repairing rotator cuff tears is also described.

Abstract: A guide assembly for facilitating placement of a fixation member within a medullary canal of a radius is provided. According to one embodiment, a guide assembly includes a guide fastener configured to attach to a fixation member and a guide member configured to receive the guide fastener such that the guide member is secured to the fixation member. The guide assembly also includes an interchangeable distal guide member configured to engage and be disengaged from the guide member. The distal guide member defines a plurality of fastener guide openings for guiding respective fasteners through a plurality of fastener openings defined in the fixation member.

Abstract: A fixation mechanism and method of fixation, such as the fixation of a facet resurfacing implant to an articular facet of a spinal vertebra. The fixation mechanism includes a securing mechanism having a socket configured to receive a knob of a biologic implant. The fixation mechanism further includes a locking mechanism for limiting expansion of the socket following engagement with the knob of the implant.