Abstract: A surgical implant according to an exemplary aspect of the present disclosure includes, among other things, a body that extends along a longitudinal axis between a drive head and a tip. The body includes a cannulation disposed about the longitudinal axis and extending from the tip to the drive head, a solid thread that wraps around the body and a porous region circumferentially extending about the body between adjacent revolutions of the solid thread. In another embodiment, the surgical implant may include a wedge having at least one porous region that extends continuously around a wedge body between an inner wall and an outer wall.

Abstract: A system and method for inserting and aligning an acetabular cup in the human pelvic bone, including selectively combining aspects of a vibratory BMD3 and an axially-impacting BMD4, including initially utilizing BMD3 vibratory insertion to partially insert and perfectly align the acetabular cup into the pelvis, and subsequently switching to a BMD4 controlled impaction technique to apply specific quantifiable forces for full seating and insertion, wherein the proven advantages of the vibratory insertion prototype with the advantages of the controlled impaction prototype are combined in a single device.

Abstract: The present invention relates generally to implants and tools for the fixation or fusion of joints or bone segments. These tools include tissue dilators and protectors. Other tools include broaches used to shape bores in bone. The tools can also include a system for removing an implant from bone. Implants can include assemblies of one or more implant structures that make possible the achievement of diverse interventions involving the fusion and/or stabilization of lumbar and sacral vertebra in a non-invasive manner, with minimal incision, and without the necessitating the removing the intervertebral disc. Implants for fusing both sacroiliac joints of a patient include a long implant that extends across both sacroiliac joints.

Abstract: Sacroiliac (SI) joint implants for promoting SI joint fusion and methods of their delivery are described herein. The SI joint implant has a spacer operatively coupled to a planar member having tapered holes to receive fastening elements. When placed in the SI joint, the spacer engages the articular surfaces of the SI joint while the plate traverses the SI joint. The implant is held in place fastening elements, which are inserted through the tapered holes in the planar member. The implant is delivered via an inferior inlet MIS procedure, wherein the SI joint is accessed through an inlet inferior to the SI joint.

Abstract: A first method, for reducing and stabilizing at least one of a fracture in, a dislocation of, and a subluxation of at least one bone, includes forming a hole in the at least one bone. The first method also includes anchoring a first portion of a cable relative to the at least one bone and positioning a second portion of the cable in the hole in the at least one bone. With the second portion of the cable positioned in the hole in the at least one bone, the method includes both tensioning the cable to a measurable and adjustable tension and, with the cable tensioned to the measurable tension, anchoring a third portion of the cable relative to the at least one bone.

Abstract: An apparatus for passing a cable through a pass-through hole in a bone that includes a hole-forming tool and a cable. The hole-forming tool has a shank, a cutting portion, and a first connection feature. The cutting portion is interposed between the shank and the first connection feature and the shank is detachably coupleable to a driving tool. The cable has a first-end portion that has a second connection feature. The cable is detachably coupleable to the hole-forming tool via the first connection feature of the hole-forming tool and the second connection feature of the first-end portion of the cable.

Abstract: A knotless suture anchor may include an anchor body with a proximal end, a distal end, an interior longitudinal passageway, a proximal opening communicating with the longitudinal passageway nearer the proximal end, and a distal opening communicating with the longitudinal passageway nearer the distal end. A first suture portion extends within the longitudinal passageway between the proximal opening and the distal opening, a second suture portion is contiguous to the first portion and extending out of the anchor body, a third suture portion is contiguous to the second portion and extends within the longitudinal passageway proximally to distally, and a fourth suture portion is contiguous to the third portion, extending along the exterior surface distally to proximally. A proximal member may be joined to the anchor body by a frangible connection and may have a proximal member axial passage containing an interference member coaxially aligned with the longitudinal passageway.

Abstract: A bone fusion method, system and device for insertion between bones that are to be fused together and/or in place of one or more of the bones, such as, for example, the vertebrae of a spinal column. The bone fusion device comprises one or more extendable tabs having a central rib. The bone fusion device includes one or more support channels configured to receive an insertion instrument that is then secured to the bone fusion device via a coupling mechanism. As a result, the coupled device is able to be securely positioned between vertebrae using the insertion instrument with minimal risk of slippage.

Abstract: The present invention relates to a polymer scaffold design and method for treating segmental long bone defects without amputation that permits permanent regrowth of bone in the area of the segmental defect, without external fixation or other problems inherent in current systems. The polymer scaffold is preferably made from a poly(ester urea) polymer and includes an outer shell, sized to fit over a segmental defect in a bone, and a collagen containing material. In some embodiments, the collagen containing material is placed in a polymer insert sized to fit within the segmental bone defect and within said outer shell. In some embodiments, the outer shell may contain struts running longitudinal struts along the inside surface of the outer shell. In some of these embodiments, the insert will have a corresponding set of grooves sized to receive the struts.

Abstract: A spinal screw assembly is provided. The assembly may be provided with a screw and a movable head in which angulation of the screw relative to the movable head is constrained so that angulation within limits is allowed in one plane but lesser or no angulation is allowed in another plane. Methods to assemble the disclosed apparatus are also disclosed.

Abstract: Surgical methods for stabilizing a joint are disclosed. The methods aid in surgical repairs by allowing for quick and reproducible repairs to be made. A bone tunnel is formed anteriorly/posteriorly in clavicle, and a bone tunnel is formed superiorly in acromion. At least one cannulated insert is provided into one or both of bone tunnels to protect the bone from abrasions caused by a flexible construct. A flexible construct is passed through the acromion tunnel and the clavicle tunnel. An attachment device may then be positioned on at least one side of the clavicle and/or acromion tunnel, and the flexible construct is attached to the attachment device.

Abstract: Disclosed are bone spacing implants for bone fusion with an open helix locking system and insertion instrumentation for implanting a spacer and fixating with a helix lock without removal of instrumentation between steps. Implanting methods comprise the steps of: positioning a coil driver over an elongate shaft portion of a bone spacer inserter; loading a helical lock implant on a distal end of an elongate shaft portion wherein an elongate shaft portion occupies a central core space of the helical lock; positioning and fixing a selected bone spacer implant to the bone spacer inserter instrument; advancing the bone spacer and helical lock instrumentation assembly into an intervertebral space; advancing through rotation a coil driver transmitting torsional forces against a butt surface of a helix lock until the helix lock is fully threaded into adjacent bone and the bone spacer.

Abstract: The invention relates to a device for trapping the end of at least one fascicle (10) of soft material in a bone tunnel (1), comprising: a ferrule (100), a screw (200) and a washer (300), the ferrule comprising a proximal upper rim (140) and screwing elements (150), with a longitudinal axis (151) inclined ? degrees in relation to the longitudinal axis (101) of the ferrule, and an inner thread (152) reciprocal to the outer thread (201) of the screw, the assembly being designed such that as the screw, with the washer, screws into the inner thread (152), the outer face (301) of the washer (300) approaches the inner face (142) of the proximal upper rim (140), an upper passage being formed between the two, via which the soft material projects, which is trapped in this way.

Abstract: Embodiments herein are generally directed to spinal implants, systems, apparatuses, and components thereof that can be used in spinal fusion and/or stabilization procedures, as well as methods of installation. The spinal implants may be expandable. In some embodiments, the spinal implants may be configured to be backfilled with bone graft material after insertion.

Abstract: A surgical instrument for assessing tissue characteristics such as tissue density and volume is disclosed. The surgical instrument is hand-held and includes transducers adapted for emitting and/or receiving acoustic signals. The surgical instrument utilizes pulse-echo to determine tissue characteristics. The surgical instrument may be utilized to determine such things as the size of a lesion and whether the lesion has been completely removed or filled with graft material.

Abstract: An arthrodesis anchor as a monolithic piece has prongs supporting barbs extending radially therefrom. A neck between the ends may be angled to accommodate final alignment of resected surfaces of joints to be bonded. The neck may receive a tool for buttressing a first inserted end against further penetration into a joint while the second inserted end is inserted into the other adjacent joint. The proximal and intermediate phalangeal joints may be trimmed and pilot drilled, and may be broached with or without a k-wire guide. A first end may be inserted by a tool, typically into the proximal joint, but the order may be reversed. The second end may then be inserted into a pilot in the base of the intermediate joint.

Abstract: A minimally invasive transforaminal lumbar interbody fusion surgery method includes sequential steps of (a), aided by a guidance system, placing a guide wire in each pedicle of each vertebra of each spinal segment to be fused in a transforaminal lumbar interbody fusion surgery, (b) replacing one or more of the guide wires with respective pedicle markers, and (c) performing the minimally invasive transforaminal lumbar interbody fusion surgery using the pedicle markers and remaining ones of the guide wires.

Abstract: Disclosed are embodiments of an articulating tool having a head that articulates and is capable of maintaining an angle for drilling or placing a fastener into a bone. The articulating tool includes a housing, an articulating head, a rotatable drive shaft, and a driver tip connected to the distal shaft portion. The articulating tool may be constructed and arranged to move between a first position and a second position, wherein in the first position and the second position the articulating head and the rotatable drive shaft are at different angles with respect to the longitudinal axis of the housing.

Abstract: Anatomic points within the body are projected outside the body through the use of extenders. The projected points may then be used for measurement, or to facilitate the selection or configuration of an implant that is to be positioned proximate the anatomic points. Such an implant may be a rod for a posterior spinal fusion system. Pedicle screws may be implanted into pedicles of the spine, and may then serve as anchors for the extenders. The extenders may have rod interfaces that receive the rod in a manner that mimics the geometry of the pedicle screws so that the selected or configured contoured rod will properly fit into engagement with the pedicle screws.

Abstract: A spinal implant comprises a plurality of members. At least one element connects the members. An agent is disposed with at least one of the members. The members and the agent are disposable between a configuration for simultaneous delivery to a surgical site and an implant configuration. Systems, spinal constructs, surgical instruments and methods are disclosed.

Abstract: A fusion cage has a first component that defines an outside surface that is configured to engage a vertebral endplate, and an interior surface. The fusion cage has a second component that defines first and second opposed surfaces. One of the first and second opposed surfaces can mate with the interior surface of the first component. The fusion cage can include vertical and lateral throughholes adapted to enhance fusion.

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 method facilitates the treatment of the spine of a patient by providing simultaneous access through at least a first opening and a second opening formed in the patient. For example, the method can include the acts of positioning the patient on a surgical table, providing the first opening into a posterior portion of the patient, providing the second opening into a lateral portion of the patient, inserting a first device through the first opening into the patient to contact the spine in a first direction that is transverse to the coronal plane of the patient, and inserting a second device through the second opening into the patient to contact the spine in a second direction that is transverse to the sagittal plane of the patient, where the first and second openings are accessible simultaneously, and, when the first and second devises are inserted into the patient, the position of the patient is stationary with respect to a portion of the table.

Abstract: Distal tip designs for bone fixation devices are disclosed. In some embodiments, a system for bone fixation includes a delivery catheter having a proximal end and a distal end; an expandable member having a proximal region and a distal region, wherein the expandable member is releasably attached about the distal end of the delivery catheter at the proximal region of the expandable member; a distal cap attached to the distal region of the expandable member to seal the expandable member; a light conducting fiber; and a light-sensitive liquid; wherein the delivery catheter has an inner void for passage of a light-sensitive liquid into the expandable member to expand the expandable member and an inner lumen for passage of the light conducting fiber into the expandable member to cure the light-sensitive liquid inside the expandable member.

Abstract: Connector assemblies are provided to couple an elongate member extending along the spinal column to a bone engaging implant engaged to the spinal column. The connector assembly includes a coupler having an implant coupling portion and an elongate member coupling portion. The positioning and orientation of the coupler relative to the implant and elongate member can be adjusted to facilitate engagement of the connector assembly between the implant and elongate member.

Abstract: An instrument for attachment to and insertion of an implant device is provided. The instrument has a handle and a pair of retaining posts extending longitudinally from a distal end of the handle. Each of the pair of retaining posts have an end dimensioned to engaged a respective threaded bore of the implant device. Also, a post drive mounted to the handle and mechanically connected to each of the retaining posts so as to engage the retaining posts simultaneously is provided.

Abstract: A cervical polyaxial bone anchor includes a shank having an integral spherical head and a receiver having an upper channel for receiving a rod and a lower seat near a lower opening for receiving a closed retainer that includes a compressible upper portion engaged with the receiver seat and an expandable lower portion capturing the shank head. An outer sleeve slidable with the receiver prohibits expansion of the retainer lower portion during operation. A compression insert engages the retainer upper portion and is in friction fit with the shank head prior to fixing of an angle of the shank with respect to the receiver.

Abstract: Systems and methods of treating spinal deformity, including one or more intervertebral implants to be introduced laterally into respective intervertebral spaces, a plurality of bone screws introduced generally laterally into vertebral bodies adjacent to the intervertebral implants and/or the intervertebral implants themselves, and a cable dimensioned to be coupled to the bone screws and manipulated to adjust and/or correct the spinal deformity.

Abstract: A method for supporting a first bone portion relative to a second bone portion can include: (a) aligning the first bone portion relative to the second bone portion, (b) forming a bore extending through the first bone portion and the second bone portion through a void defined by opposing surfaces of the first and second bone portions after the aligning of the first bone portion with the second bone portion, (c) disposing a pin in the bore to span the void, wherein the pin includes a coupler, (d) drawing a self-locking, adjustable suture construct coupled to the coupler through the bore by withdrawing the pin from the bore, and (e) compressing the first bone portion and the second bone portion between a first anchor and a second anchor coupled to the suture construct by tensioning the suture construct.

Abstract: The present invention relates to a device for fixation of bone fragments at bone fractures. The device comprises at least two fixation means (5, 6) and a securing plate (4). With the object of preventing or counteracting re-dislocation, the respective fixation means (5, 6) each have a first fixing portion (19) for fixing the fixation means in an inner bone fragment (3), a second fixing portion (21) for locking the fixation means to the securing plate (4) which is disposed on the outside of an outer bone fragment (2) and allows movement of the outer bone fragment relative to it, so that the fixation means are prevented from changing their angular position relative to the securing plate and relative to one another, and a middle portion (22) which is situated between the fixing portions and runs through the outer bone fragment, along which middle portion the outer bone fragment can slide inwards towards the inner bone fragment in which the fixation means is fixed.

Abstract: Stand-alone interbody fusion devices for engagement between adjacent vertebrae. The stand-alone interbody fusion devices may include frames and one or more endplates coupled to the frame. The frame may be configured and designed to provide the apertures which are designed to retain bone fasteners, such as screws or anchors, and secure the implant to the adjacent vertebrae.

Abstract: A device for treating a bone includes (a) an elongate body sized and shaped for insertion into a bone and extending longitudinally from a proximal end to a distal end, the elongate body including a channel extending therethrough and a coating along an outer surface thereof, the coating adapted to absorb a selected frequency of light such that, when the selected frequency of light is applied thereto, portions of the coating melt to form a mass; and (b) a first anchor member slidably mountable over the elongate body and movable therealong from a first position at the proximal end of the elongate body to a second position adjacent a bone into which the elongate body has been inserted to cooperate with the mass to fix the elongate body to the bone.

Abstract: The present invention generally is directed toward a spinal fixation system whereby a coupling element allows the physician to selectively lock or unlock either the connection between the coupling element and a fastener, such as to allow for repositioning of the coupling element, or the connection between the coupling element and an elongate rod. The locking or unlocking of these connections may be made independently and as desired by the physician.

Abstract: A method of limiting at least one degree of movement between a superior vertebral body and an inferior vertebral body of a patient includes advancing a distal end of a stabilization device into a pedicle of the inferior vertebral body. A proximal portion of the stabilization device is positioned such that the proximal portion limits at least one degree of movement between a superior vertebral body and an inferior vertebral body by contacting a surface of the superior vertebral body.

Abstract: The present invention generally is directed toward a spinal fixation system whereby a coupling element allows the physician to selectively lock or unlock either the connection between the coupling element and a fastener, such as to allow for repositioning of the coupling element, or the connection between the coupling element and an elongate rod. The locking or unlocking of these connections may be made independently and as desired by the physician.

Abstract: A modular dental implant including a body portion, a sleeve, and an end cap. The sleeve may be formed of porous material, such as a porous metal material to promote bone ingrowth. The sleeve is positionable around a core of the body portion and the end cap is attached to the core of the body portion such that the sleeve is positioned between the head of the body portion and the end cap. The sleeve includes one or more anti-rotation features formed in the upper surface and/or lower surface of the sleeve configured to interact with one or more anti-rotation features formed in the lower surface of the head of the body portion and/or the upper surface of the end cap which prevent rotation of the sleeve relative to the core of the body portion.

Abstract: A porous tantalum rod is provided, which is a medical implantation used for treating collapsed articular surface of the femoral head or necrosis of the femoral head in phase I or phase II. The implantation includes a fastening structure formed on one end of the porous tantalum rod used for connecting with the osseous tissues and a through hole formed on the center of the porous tantalum rod. The porous tantalum rod is made of the porous tantalum material, which is produced by foam impregnation and had a foam structure with three-dimensional interconnecting pores, wherein the foam structure has a foam skeleton, tantalum particles located on the foam skeleton, and multiple sintering neck structures formed between the tantalum particles.

Abstract: A spinal correction apparatus comprises a body. A ratchet is disposed with the body. A longitudinal element is connected to the ratchet. A force is applied to at least a portion of the apparatus that causes dynamic incremental movement of the longitudinal element relative to the body in at least one direction. Methods of use are disclosed.

Abstract: A vascular occlusion, flow restriction, shunt or filter device is disclosed comprising the assembly of at least two, of a number of selectable discrete interconnectable, interchangeable components, at least one component being of the type fabricated from metal strands braided into a tubular metal fabric having an expanded preset configuration and an elongated, collapsed reduced diameter configuration for delivery through a catheter to a treatment site and the device shaped to create an occlusion, flow restriction or shunt when placed in an opening in a body organ or vessel, the woven metal fabric having a memory property whereby the medical device tends to return to said expanded preset configuration when unconstrained.

Abstract: A fusion cage has a first component that defines an outside surface that is configured to engage a vertebral endplate, and an interior surface. The fusion cage has a second component that defines first and second opposed surfaces. One of the first and second opposed surfaces can mate with the interior surface of the first component. The fusion cage can include vertical and lateral throughholes adapted to enhance fusion.

Abstract: Correction of a scoliotic curve in a spine comprises the steps of implanting an expanding rod isolated completely under the skin and attached to selected portions of the scoliotic curve of the spine at opposing ends of the rod; and producing a controlled force by means of expansion of the rod over at an extended time period under external control until a desire spinal curve is obtained. An incremental force is generated to stretch the scoliotic curve of the spine between the selected portions where attachment of the rod is defined. The controlled force is provided steadily for at least one month or alternatively 1-3 months. Multiple rods may be employed each associated with a different scoliotic curve of the spine or a different portion of the scoliotic curve.

Abstract: In one embodiment, a device for measuring a length of a bone tunnel is provided. The device includes: a gauge comprising an annular shaft coupled to a handle, the handle including a constrained channel configured for receiving a passing pin from the annular shaft and displaying the passing pin in relation to a scale. In another embodiment, a method for measuring length of the bone tunnel is provided. A method and another device are provided.

Abstract: An implant (1) for attaching the first implant (1) to a tubular bone, in particular a rib bone, includes: a clamp (10) having a fillet (100) and prongs (101, 102, 103) extending from the fillet (100); and a first connecting element (11) for connecting the first implant (1) to a connector implant. The clamp (10) and the connecting element (11) are connected so as to be rotatable relative to each other about an axis.

Abstract: A bone clamping system includes a shaft (3), a first plate (1) integrally attached to the shaft and a second, movable plate (20), wherein a locking leaf (22, 23), penetrating into the shaft (3) or not, locks the second plate (20) on the shaft (3).

Abstract: Embodiments provide a method and device for plate osteosynthesis of a bone fracture that allows angle-stable fixation of the bone fracture, while permitting elastic axial motion at the fracture site in a controlled, symmetric manner to stimulate fracture healing. Embodiments pertain to a bone plate having an outer surface and a bone-facing surface. The bone plate incorporating internal sliding elements containing a threaded receiving hole for bone screws that have a correspondingly threaded screw head. The sliding elements undergo controlled displacement parallel to the longitudinal axis of the plate but are substantially constrained against displacement perpendicular to the longitudinal axis of the plate. The bone screws with threaded heads may be rigidly fixed to the threaded receiving holes in the sliding elements without compressing the bone plate onto the bone surface. Sliding elements are elastically suspended inside the bone plate and undergo dynamic motion.

Abstract: An assembly for distraction of spinal vertebrae and which can optionally accommodate retraction blades. The assembly includes a pair of pins each having a first end adapted for vertebral bone engagement and a second end. A pair of sleeves respectively and concentrically engage said pins. A frame includes respective openings which receive the pins and a first end of each said sleeves. The first end of each said sleeve including a portion offset relative to a longitudinal axis of said sleeve such that when the first end of each said pins is anchored in bone, axial rotation of each said sleeves enables said first end of each said pins to move between a first position in which said vertebral bones are not distracted and a second position in which said vertebral bones are distracted.

Abstract: In one embodiment, a fixation system includes an anchor adapted to be implanted within a first bone, a washer adapted to be associated with a second bone that is to be secured to the first bone, and a suture that is fixedly attached at one end to the anchor and that extends between the anchor and the washer in multiple passes, the suture being adapted to extend through a passage formed in the first and second bones.

Abstract: According to an aspect of the invention, in a set of male dental components, such as abutment screws, each male dental component has a threaded portion with different core diameter. Each male dental component is to be connected to a mating female dental component, such as an abutment. The smaller core diameter a threaded portion has, the higher friction is provided when the male dental component is finally tightened to its mating female dental component, even though the same insertion torque is applied to all male dental components.

Abstract: A method and apparatus for bunion repair using a suture passing K-wire configured to easily pass through bone tunnels with suture trailing. The suture passing K-wire includes a tapered guide pin with a multi-diameter shaft (i.e., comprising at least two regions or sections that have different diameters) and a loop which is securely attached to an end of the guide pin (i.e., to the smaller diameter section of the guide pin). The reconstruction system may be formed of a pair of buttons connected by a flexible strand. The procedure offers indirect placement of buttons and a minimally invasive approach.

Abstract: A coupling device for securing an elongate member to the spine is provided. The coupling device comprises a compressible inner member that secures an anchor member therein when the inner member is axially shifted within an outer member. The elongate member is retained within the device by an axially inserted locking member, and may be secured independently of the anchor member. The coupling device and anchor may be configured to provide increased angulation of the anchor with respect to the coupling device. For instance, anchor member may have an offset head portion in order to provide normal pivoting of the coupling device when the anchor is attached to bone at an angle.