Abstract: The positioning device for bone drilling comprises a base, and the base has an outer wall, a positioning block, a guiding recess and an inner wall. The positioning block is formed on the outer wall of the base. The guiding recess is formed longitudinally through the base. The inner wall surrounds the guiding recess and the inner wall is a concave camber. The doctor can use the positioning block to fix the positioning device on a guide mold. A relative position between the positioning device and the guide mold can be relatively fixed. Prior to or during the drilling, the doctor can replace the positioning device with another positioning device with a more suitable diameter, oblique angle and oblique direction so that the positioning device for bone drilling can drill a hole at an accurate position, at an accurate oblique angle and in an accurate oblique direction as desired.

Abstract: A device for osteosynthesis includes a body having a proximal surface, a distal surface configured and dimensioned to face a target portion of bone over which the body is to be mounted and a through opening extending through the body from the proximal surface to the distal surface along a central axis. The through hole includes a first protrusion extending from an inner surface thereof toward the central axis. The first protrusion is biased toward an unstressed state in which the first protrusion extends into the through opening to a first distance from the central axis. The first protrusion is movable toward the inner surface when subjected to a force directed outward from the central axis.

Abstract: A single use bone cutter comprised of a plate with a plurality of insert blade enclosures is described. The insert blade enclosures are arranged in a spiral pattern about the plate and are further positioned at varying height intervals through the thickness of the plate. The bone cutter provides a means whereby the insert blades can be easily positioned within the plurality of blade enclosures to provide a wide array of cutting diameters.

Abstract: A technique for locating an axis of a bone, which extends through the center of rotation of the bone around a joint between that bone and another bone, involves a. moving the bone in a plane about the said joint, between a first point and a second point, b. locating a third point which is equidistant from the first and second points, and c. locating the axis which passes through the third point, perpendicular to a line which connects the first and second points. The invention provides an instrument for performing this technique.

Abstract: A method and apparatus assisting safe one-handed insertion of an implant. An implant implantation device has a frame which includes a trigger mechanism, an outer sleeve mechanically coupled to the frame, an inner shaft having a grabber for mechanically engaging an implant, the inner shaft slidably disposed within the outer sleeve, and a retaining element disposed over the inner shaft for directing the grabber toward a closed position. An implant clip has a first member, a second member pivotally coupled to the first member, a first implant holder pivotally coupled to the first member, the coupling causing the implant clip to have a closed position and an open position, and a second implant holder, the second implant holder pivotally coupled to the second member, a surface of the first implant holder and a surface of the second implant holder remaining substantially parallel to each other while the first member and the second member pivot between the closed position and the open position.

Abstract: An anchor includes an anchor body configured to be retained within base tissue. The anchor body includes a unidirectional mechanism to selectively restrict passage of a flexible member through the anchor. The flexible member includes a loop to enable attachment of candidate tissue to base tissue without the use of knots.

Abstract: A sternal reconstruction system for securing parts of a sternum includes at least one flexible cable with a fused end fitting, at least one parallel fitting piece and at least one ferrule. Optionally, the system includes at least one cannulated screw. Circumferential or parasternal fixation may be brought about by use of the sternal reconstruction system. Also provided is a method for sternal reconstruction utilizing the sternal reconstruction system. Also provided is a kit for sternal reconstruction.

Abstract: A method of using a guide system for resecting a bone through incisions of the type utilized for arthroscopic procedures is provided. The guide system comprises a first alignment pin, a second alignment pin and a wire saw. The first alignment pin is configured to be inserted through a first incision into a bone in a first orientation. The second alignment pin is configured to inserted through a second incision into the bone in a second orientation. The first alignment pin and the second alignment pin are configured and oriented to define a resection plane of reference through which the bone is to be resected and the wire saw is configured to be inserted through the first and second incisions to be guided by the first and second alignment pins while being moved to resect the bone.

Abstract: Methods are described wherein bone constructs of a patient are used to arthroscopically attach sutures to torn or dysfunctional tissue. A suture or multiple sutures are passed through intersecting/bisecting tunnels formed in the bone. An end of the suture extends from each of the tunnels, and the ends are used to secure the tissue to the bone, such as by arthroscopic tying of the ends, and pulling the tissue against the bone. Devices for performing the methods are also described.

Abstract: A plurality of osteotomes that are linked together via a recess and a matching projection such that the osteotomes remain linked when used to manipulate bone.

Abstract: Methods for fixation of a soft tissue graft in a bone including: forming in the bone a tunnel defining an entrance opening and an exit opening at opposite ends of the tunnel, the tunnel including an anterior wall surface and a posterior wall surface opposite to the anterior wall surface; positioning the soft tissue graft within the tunnel such that the soft tissue graft extends through both the entrance opening and the exit opening of the tunnel; inserting a graft fixation apparatus into the tunnel and driving spikes of the graft fixation apparatus into the posterior wall surface to mount the graft fixation apparatus to the posterior wall surface of the tunnel such that the graft fixation apparatus is anterior to the posterior wall surface and is not recessed beneath the posterior wall surface; and securing the soft tissue graft inside the tunnel with the graft fixation apparatus.

Abstract: The present invention relates to a tool in combination with a set screw for use in spinal implant systems, and more particularly to a tool for the deployment of set screws with a break-off neck portion comprising a handle portion, a stem portion extending from the handle portion, a set screw retaining means, and a driving means extending from the stem portion and disposed opposite the handle portion. The driving means is adapted to allow the installation of the set screw to the bone and applying torque for the shearing of the neck portion thereof, and at the same time is adapted to remove the installed screw portion of the said set screw when needed.

Abstract: Spinal anchoring methods and devices are provided that are effective to correct spinal deformities while allowing some flexibility to the spinal. In particular, the methods and devices allow a spinal fixation element to mate to several adjacent vertebrae to maintain the vertebrae at a fixed distance relative to one another, yet to allow the orientation of each vertebrae relative to the fixation element to adjust as the orientation of the patient's spine changes.

Abstract: A method for preparing a femur for receiving a prosthesis can include positioning an intramedullary (IM) member in the femur. A femoral trial component can be positioned onto a distal end of the femur. The femoral trial component can have an attachment portion and at least two cut surfaces thereon. A modular boss assembly can be attached to the attachment portion of the femoral trial component. The modular boss assembly can have a boss stem that is configured to operably connect to the IM member. A desired contact between the femoral trial component and the distal femur can be confirmed based on the attaching. The femoral trial component can be fixed to the distal femur based on the confirming. The modular boss assembly can be removed from the femoral trial component. A reamer bushing can be coupled relative to the femoral trial component.

Abstract: A reamer for use in performing arthroplasty includes a first cutting structure having an inner concave surface that defines a first cavity and terminates in a generally circular leading edge. The inner concave surface includes a first cutting feature that is spaced apart from the leading edge. An elongate member extends from the first cutting structure into the first cavity toward the leading edge that includes a second cutting feature. A second cutting structure is secured to the elongate member and positioned within the first cavity. The second cutting structure extends outwardly from the elongate member toward the inner concave surface and includes a third cutting feature.

Abstract: A method is provided for delivering an implant for replacing a portion of an articular surface. The method may include forming a socket in an articulating feature that is capable of moving relative to the articular surface. An implant may be placed in the socket and the articulating feature may be moved relative to the articular surface to generally align the socket with an implant site formed in the articular surface. The implant may be transferred from the socket into the implant site.

Abstract: An implantable spinal cross connector is provided for connecting one or more spinal fixation devices, and more preferably for connecting two spinal fixation rods that are implanted within a patient's spinal system. In general, an exemplary cross connector in accordance with the present invention includes an elongate body with at least one rod-receiving recess formed therein, and a locking mechanism that is adapted to couple to the elongate body and that is effective to lock a spinal fixation rod within the rod-receiving recess(es). The present invention also provides an inserter tool to facilitate implanting a spinal implant or device, such as a spinal cross connector.

Abstract: A system and method for a multi-axial connection of an apparatus to bone. The system may include a fastener inserted into a body and a head of the fastener held within a chamber of the body through a combination of a retention ring, a pressure cap, a rod, and a compression element. The compression element applies force to the rod which, in turn, pushed on the pressure cap. The force on the pressure cap urges it against the head of the fastener and pushed it against the retention ring. The force on the retention ring causes it to expand to the walls of the chamber. Once the ring can no longer expand within the chamber, the head of the fastener is wedged between the retention ring and the pressure cap.

Abstract: Implants for forming a positive connection with human or animal parts include a material, such as thermoplastics and thixotropic materials, that can be liquefied by means of mechanical energy. The implants are brought into contact with the tissue part, are subjected to the action of ultrasonic energy while being pressed against the tissue part. The liquefiable material liquefies and is pressed into openings or surface asperities of the tissue part so that, once solidified, the implant is positively joined thereto. The implantation involves the use of an implantation device that includes a generator, an oscillating element, and a resonator. The generator causes the oscillating element to mechanically oscillate, and the element transmits the oscillations to the resonator. The resonator is used to press the implant against the tissue part to transmit oscillations to the implant.

Abstract: An instrument for measuring the medullary canal of a long bone in order to determine the proper size for a stem centralizer is provided. The instrument includes an elongated central portion defining opposed first and second ends and a contact portion. The contact portion extends from the first end or the second end of the elongated central portion. The contact portion has a contact area for contact with the medullary canal and defines a relief area for providing clearance between the instrument and the medullary canal.