Abstract: Disclosed is a drug delivery implant implanted into a bone. The drug delivery implant includes an implant fixture provided with an inlet formed at the upper end thereof and a drug supply cartridge coupled to the fixture, the drug supply cartridge includes a cap to close the inlet of the fixture and a cartridge main body provided under the cap, coupled with the cap and accommodated in the fixture to release a drug, and a cartridge hole to accommodate the cartridge main body and drug channels to guide the drug released from the inside of the cartridge main body to the outside of the fixture are formed in the fixture. The drug delivery implant may continuously administer the drug into bone tissues and mount the drug cartridge together with the cap in the fixture, thus facilitating mount of the drug cartridge in the fixture and replacement of the drug cartridge.

Abstract: The present disclosure relates to an interference screw for creating an interference fit between a bone tunnel and tissue. The screw includes a threaded body having a proximal end, distal end, and thread extending around the threaded body between the proximal and distal ends. A supporting spline extends along a cannulation through the threaded body. The supporting spline is engagable with a delivery device. The screw further includes at least one opening defined by a surface between threads of the threaded body. A ratio of open surface area to closed surface area defines the opening and is selected such that, when torsionally loaded, the screw does not exhibit plastic deformation when inserted into an undersized bone tunnel. The screw further includes a tapered tip extending from the distal end of the threaded body. The tapered tip has a thread extending at least partway around the tapered tip.

Abstract: An intervertebral implant comprises first and second parts having outer surfaces engaging adjacent vertebral surfaces. An insert between these parts provides relative movement therebetween. The first and/or second parts may have engagement means in the form of apertures for engagement with insertion instruments. The first and second parts may nest together, in the absence of the insert, for insertion into the intervertebral space. The boundaries of the implant may form a working space which would include insertion instruments therein. A detent and detent recess may be provided for engagement of the insert and one of said first and second parts.

Abstract: An osteosynthesis system for treating fractures of tubular bones includes an intramedullary nail with an elongated nail body consisting of a hard metal material with two end sections and a middle section that has at least one transverse screw hole close to the end for screwing in at least one bone screw into each end section. The nail body has a through-channel for pushing through a guide element, in the middle section on the side of the through-channel with the lowest wall thickness, at least two transverse one-sided screw holes for screwing in bone screws are placed proximate to a fracture, all one-sided screw holes are formed as inlays made out of soft metal material securely joined to the nail body, and bone screws with an initial thread consisting of hard metal material that can be screwed into the bone and screw holes while forming threads.

Abstract: A bionic fixing apparatus is provided. The bionic fixing apparatus includes a flexible portion having at least one trench. The trench is disposed on the surface of the flexible portion and has a first end and a second end. An interval is disposed between the first end and the second end. The trench is disposed for spreading the stress applied on the bionic fixing apparatus and preventing stress concentration and stress shielding.

Abstract: The apparatus and method is directed to a pair of self-tapping, interconnecting, externally and internally threaded devices that, when installed between two separate pieces of material, will draw and hold the material together as a single threaded unit. While the pair of threaded devices are being fastened into the host material, due to the unique design of their threads, no radial outward forces are produced that could cause cracking or splitting of the sections of the material into which they are installed. The external threads are helically defined into the exterior of each half of the device with a right hand thread defined into one half and a left hand thread into the other half. When the two halves are being fastened together, the increased thread pitch on one of the halves continuously draws the halves into each other even when the internal threads have already been maximally tightened.

Abstract: A surgical implant comprising a screw element having a screw head, a first thread having a first thread pitch, a second thread having a second thread pitch and an intermediate portion coupling the first and second thread pitches with the first and second thread pitches being different. The implant has a buttressing head associated with the first thread, and it is dimensioned to be larger than a diameter of the first threads to provide external buttressing as the first and second threads compress a first bone and a second bone together.

Abstract: A bone fastener includes a fixation portion configured to interface with boney tissue, a connection portion having a longitudinal axis and being configured to interface with an elongated support structure, and a flexible portion disposed between the fixation portion and the connection portion. The flexible portion is configured to permit flexure of the connection portion relative to the fixation portion. The flexible portion has a first set of opposed facing surfaces that mechanically limit the range of flexure in a first direction. It has a second set of opposed facing surfaces that mechanically limit the range of flexure in a second direction. The opposed facing surfaces are substantially transverse to the longitudinal axis.

Abstract: A radially expandable sheath is provided having a substantially closed distal end with at least two sidewalls extending proximally therefrom and defining a central lumen. Each sidewall can have a substantially concave outer surface adapted to seat a graft member, and each side wall is at least partially separated by a longitudinally oriented slot that extends from a proximal end along a substantial length of each sidewall. The slot preferably terminates at a position just proximal to the distal end. The device can also include a sheath expander that is adapted to be disposed in the central lumen of the radially expandable sheath and that is configured to flex the sidewalls to radially expand the sheath so as to fix a graft member within a bone tunnel.

Abstract: A multi-axial expandable pedicle screw includes a hollow screw having a spherical shaped end for connecting with an adapting piece in the form of a universal joint structure. The hollow screw further includes a tip shaped end, and a bore formed inside the hollow structure having a taper shaped tip. Expansion gaps are formed in the hollow screw to uniformly set up two, three, four or more anterior fins on the hollow screw extending upward along its axial direction, from its tip to the bore. The hollow screw is configured to receive an inner needle disposed in the bore. This pedicle screw is easy to operate and provides a high degree of control in screw expansion with increased stability and reliability. At the same time, this pedicle screw reduces the occurrence of screw loosening, and screw pull-out events, and also reduces failure rates of spinal surgeries.

Abstract: A composite fixation device is described herein which includes a first and second biodegradable material. The first and second biodegradable materials degrade at different rates thereby permitting tissue ingrowth into the device prior to degradation of the entire device.

Abstract: Improved bone screws are provided. The bone screws comprise a head portion that is connected to a shaft portion. The shaft portion can comprise one or more fenestrations that extend along a length of the screw. The fenestrations can be straight, or they can include angled bends and arcuate curves. At least a portion of the bone screws can be shot-peened or cold-worked in order to increase the strength of the bone screws to allow for use in, among other regions, the cervical region of the spine.

Abstract: Present invention depicts a poly-porous (micropore) hollow screws as diffusion chamber filled with core matrix for targeted delivery of growth factors and bone marrow stem cells. The screws comprise at least two parts: the distal part of the screw consists of the tip of the screw made of poly porous material and hollow inside proximally. It has threaded navel attached to the threaded nipple of the distal part of the proximal screw which has the screw head and is made of the solid material of the same kind. The screw head had hexagonal recess targeted for screw driver insertion. Assembly of screw created a chamber in the middle of the screw. The chamber is filled with core matrix consisting of gelatin nano-particles pre-impregnated with BMPs (BMP2/BMP7 for bone or BMP12 for tendon, ligament) and fibrin sealants or Chitosan dispersed with bone marrow stem cells and/or other growth factors. Bioactive protein core material is prepared during the surgery and filled the chamber of the screw by the surgeon.

Abstract: An inserter for inserting a suture anchor into bone. The inserter has external markings that uniquely identify the orientations and the relative longitudinal positions of at least two suture passages through a suture anchor releasably engaged with the inserter. The markings assist a surgeon in determining a preferred placement and orientation of the anchor at an operative site during a surgical procedure.

Abstract: A bone screw includes a head portion and shank portion. The shank portion includes a regularly outwardly expanding threaded portion.

Abstract: An absorbable screw fastener and a method of firing with an applicator capable of applying a surgical fastener to tissue in order to form tissue connection to secure objects to tissue, the fastener including a body portion having a helical thread, a head portion disposed at the proximal end of the body portion. The head portion includes a driver receiving configuration on its outer surface. The screw fastener further includes a cannulated center lumen with an opening extending from the head portion through the longitudinal length of the body portion.

Abstract: A bone anchoring nail is provided having a threadless shaft with a free end, a head opposite to the free end, the head having a substantially U-shaped recess for accommodation of a rod or a rod-shaped element, a longitudinal bore extending through the shaft and opening towards any one of the head and the free end and a plurality of openings extending through the wall of the shaft and being in communication with the bore. The bone anchoring nail allows quick insertion and reliable fixation enhanced by the in-growth of blood vessels.

Abstract: The various embodiments of the present invention provide a system, including methods, apparatus and kits for connecting bones and/or bone portions using a multi-part bone connector with one or more rotating joints.

Abstract: A bone fixation device includes one or more springs and one or more spacers disposed between two orthopedic structures. The orthopedic structures may comprise screws, rods, plates, or any other orthopedic devices configured to engage bone. The spacer may be absorbable or removable, and may serve to constrain the spring in a compressed or stretched state so that, upon absorption or removal of the spacer, the spring may apply tension or compression to surrounding bone. The device may thereby facilitate healing or bone or remodeling of soft tissues.

Abstract: A bone screw includes a head portion and shank portion. The shank portion includes a regularly outwardly expanding threaded portion.

Abstract: An inserter for inserting a suture anchor into bone. The inserter has external markings that uniquely identify the orientations and the relative longitudinal positions of at least two suture passages through a suture anchor releasably engaged with the inserter. The markings assist a surgeon in determining a preferred placement and orientation of the anchor at an operative site during a surgical procedure.

Abstract: A surgical screw that includes a body portion that facilitates bone in-growth from a bone in which the screw is mounted so as to stabilize the screw in the bone. The body portion can have various configurations for facilitating bone in-growth, such as indentations, a roughened surface, such as by acid etching or abrasive media blasting, specialized coatings, such as hydroxyapetite, sintered beads, machined channels, etc. Because the body portion of the screw facilitates bone growth, the screw will be more firmly mounted to the bone so as to have a greater integrity in response to movement of the bone. The type of surgical screw can be any surgical screw that will benefit from being better anchored in bone, such as pedicle screws, long bone screws, cervical fusion screws, tendon anchoring screws, etc.

Abstract: A composite fixation device is described herein which includes a first and second biodegradable material. The first and second biodegradable materials degrade at different rates thereby permitting tissue ingrowth into the device prior to degradation of the entire device.

Abstract: An expandable osteosynthesis implant has branches each connected at one end to a seat which is pierced by an orifice, suitable for being slid from a posterior direction between the facing faces of two consecutive vertebrae in order to hold them a given distance apart and restore stability of the spinal column. The branches and the seat define a hollow cage which, in a “rest” position, has an outside general shape that is a cylinder of circular section, and a portion at least of the inside volume of the cage towards the distal ends of the branches is in the form of a circular truncated cone whose large base is towards the seat, which implant has at least three branches and, inside the inside volume at least one spacer suitable for passing through the orifice and the large base of the truncated cone.

Abstract: A dynamic stabilization construct for implantation within the spine comprises bone anchors that include a flexible portion between the bone engaging and head portions of the anchor. The head portion is configured to mate with different types of stabilization elements adapted to span between spinal motion segments. The engagement portion can also be configured for different types of fixation to a motion segment, such as within the pedicle of a vertebra. The flexible portion permits limited bending of the bone anchor beneath the level of the stabilization element. In one embodiment, the flexible portion is integrated into the body of the bone anchor in the form of hinge elements. In another embodiment, a separate flexible element, such as a spacer or spring, is interposed between the head and engagement portions. In a further embodiment, the bone anchor includes a portion having a reduced cross-section.

Abstract: A bone anchor system anchors a support member to a bone. The bone anchor system comprises a body having a shank adapted for insertion into a hole in the bone. A head is formed on the shank. The head has a support engagement portion adapted to secure the support member to the body. A passage extends from an entry point to an exit point formed in the body. An expandable member has a flexible wall at least partially enclosing an anchoring chamber. The expandable member has an expanded state configured to conform to a cavity in the bone. The anchoring chamber is in fluid communication with the exit point. The expandable member is adapted to expand when a filler material is provided into the anchoring chamber. A portion of the expandable member conforms to the cavity and the body and the support member are substantially anchored to the bone.

Abstract: A cannula has a flange and a body with slots extending through the entire flange and into the body. The cannula may also have a longitudinal slot extending its entire length. An obturator used with the cannula may also have a longitudinal slot extending along its length. A surgical method using these instruments includes separating lengths of suture and managing the suture by placing lengths of suture in the slots in the cannula. The cannula and obturator may be used after suture is already in place by placing the suture in the longitudinal slots and then introducing the cannula and obturator to the tissue defect site. The cannula may also be used to deliver a therapeutic implant to the tissue defect site. The instruments and method may be used in mensical surgery.

Abstract: An absorbable screw fastener and a method of firing with an applicator capable of applying a surgical fastener to tissue in order to form tissue connection to secure objects to tissue, the fastener including a body portion having a helical thread, a head portion disposed at the proximal end of the body portion. The head portion includes a driver receiving configuration on its outer surface. The screw fastener further includes a cannulated center lumen with an opening extending from the head portion through the longitudinal length of the body portion.

Abstract: A screw for use with vertebral members having one or more slots that extend along at least a section of the length. The slots are sized to contain bone growth material. A portion of the screw length may also include threads to assist in inserting and anchoring the screw into a vertebral member. In use, the bone growth material is loaded into one or more of the slots. Once loaded, the screw may be inserted into the vertebral member to a predetermined depth. At this depth, the slots deliver the bone growth material to a position to allow for bone growth to occur.

Abstract: A bone anchoring device includes a shank to be anchored in a bone or vertebra, a head, and a receiving part receiving the head for connecting the shank to a rod. The shank and the head are separate parts. The head has a bore with a cylindrical inner surface, a ring-shaped groove provided on the inner surface, and at least one slit extending from the inner surface to the outer surface of the head. The shank has a first portion for anchoring in the bone or vertebra and a second portion with a cylindrical outer surface adjoining a free end. A projection is provided on the cylindrical outer surface which engages with the ring-shaped groove of the head, when the cylindrical second portion of the shank is inserted in the bore of the head.

Abstract: This document discusses, among other things, fiducial marker devices, tools, and methods. One example illustrates a combined computed tomography (CT) imagable fiducial locator head, an integral bone screw, and an integral divot for receiving a positioning wand of an image-guided surgical (IGS) workstation. A further example includes a fluid/gel-absorbing coating or cover into which a magnetic resonance (MR) imagable fluid is introduced, thereby permitting both CT and MR imaging. Protective caps and collars may be used to protect the fiducial marker from mechanical impact and/or to guide the fiducial marker during affixation. A bull's-eye or other template is used to select a center of a substantially spherical fiducial marker head on an image, such as for use during patient registration.