Abstract: A method for manufacturing a spherical cage. The method includes providing a wire braid and inserting a spherical ball inside the wire braid. The wire braid and spherical ball are placed inside a mold. Excess wire braid is trimmed from the mold, creating trimmed ends of the braid. The mold is heat set with the spherical ball and wire braid. The spherical ball and wire braid are removed from the ball and the spherical ball is removed from the wire braid, resulting in a spherical wire cage.

Abstract: A nail assembly for use in trauma surgery is provided. The nail assembly includes an intramedullary shaft including a first transverse passage and a second transverse passage in the shaft. The first transverse passage and the second transverse passage do not contact each other on the shaft. The nail assembly also includes a first shaft extending through the first transverse passage in the intramedullary shaft and a second shaft extending through the second transverse passage in the intramedullary shaft. The second shaft includes an engagement feature configured to bring the second shaft into contact with the first shaft. The engagement feature may be in the form of a lateral mechanical feature that provides simultaneous unilateral coupled motion of the first shaft with the second shaft through the transverse passages in the intramedullary shaft.

Abstract: An instrument for preparing a cavity for a stem of a prosthetic implant for use in performing joint arthroplasty on a head of a long bone is provided. The instrument includes a body and a punch extending from the body. The punch includes a portion of the punch having a shape similar to the stem of the implant.

Abstract: A prosthetic knee system includes a tibial tray, a non-rotating tibial insert, and a rotating tibial insert. The non-rotating tibial insert and the rotating tibial insert are selectively coupleable to the tibial tray such that a fixed or a mobile orthopaedic prosthesis may be configured. In some embodiments, the tibial tray may be a fixed or mobile tibial tray. Additionally, in some embodiments, the prosthetic knee system may include a femoral component.

Abstract: A medical procedure for use in connection with a patient suffering from cuff tear arthropathy is disclosed. The medial procedure includes providing a humeral prosthesis having a prosthetic head component, wherein (i) the prosthetic head component includes a glenoid-bearing portion and an acromion-bearing portion, and (ii) the glenoid-bearing portion and the acromion-bearing portion define an outer bearing surface, and (iii) the outer bearing surface extends in a medial/lateral direction across a radial distance D, and (iii) D?190°. The medical procedure further includes implanting the humeral prosthesis in the patient so that the acromion-bearing portion contacts and bears directly against a natural acromion of the patient during abduction of an arm of the patient that possesses the humerus.

Abstract: An apparatus for treating a bone fracture comprises an intramedullary rod extending through a first bone segment of a fractured bone. A lag screw assembly extends through a first transverse aperture in the rod, while a control member extends through a second transverse aperture longitudinally offset from the first aperture. The lag screw assembly includes a lag screw engaged to the second bone segment and a locking sleeve mounted over a proximal portion of the lag screw. The locking sleeve defines a groove aligned with the second aperture. The control member includes a distal portion penetrating the bone segments, an intermediate portion configured to engage the second aperture. and an enlarged head configured to slidably engage the groove. The groove includes a terminus that contacts the head of the control member after a predetermined amount of lateral migration of the lag screw as the fracture collapses.

Abstract: A modular implant system includes a set of anatomically-designed diaphyseal fitting and filling modular implant components and collars. The diaphyseal component connects with a selected intramedullary stem and with a selected collar component. The collar component connects to another implant component such as a modular articular component, a segmental component or an intercalary component. The diaphyseal component has a tapered porous surface that is received with a tapered bore in the bone diaphysis that is prepared to match the size and shape of the tapered porous surface. The collar component has a porous surface for tissue ingrowth, such as the periosteum, to seal the intramedullary canal. The diaphyseal implant is easy to insert and remove, does not bind before fully seating to prevent stress shielding, and eliminates the long lever arm created when fixation occurs only at the tip of the stem, and should eliminate related stem loosening.

Abstract: An apparatus for transcutaneously transferring an amount of energy to an implantable orthopaedic device includes a primary coil. The primary coil has a resonant frequency matched to a resonant frequency of a secondary coil, which may form part of the implantable orthopaedic device. The primary coil may have an aperture configured to receive a portion of a patient's body or may include a substantially “C”-shaped core. A power circuit may be coupled with the primary coil to provide power to the coil. The apparatus may also include a wireless receiver, a measuring device, and/or a display.

Abstract: Methods and devices are provided for regenerating a meniscus. The devices comprise a layer of toughened naturally occurring extracellular matrix. The devices may, optionally, further comprise a biologic material to provide a framework for meniscus regeneration. The methods comprise the steps of removing a portion of a meniscus to provide a space, and inserting a device comprising a layer of toughened naturally occurring extracellular matrix into the space.

Abstract: An orthopaedic implant includes a patella component having a posterior bearing surface configured to articulate with the femoral condyles of a femur, and an anterior surface having a number of pegs extending outwardly therefrom. The superior edge of the patella component is thickened relative to conventional dome-shaped patella components.

Abstract: A tibial tray assembly includes a platform having a stem extending downwardly from a bottom surface and a stem extension couple to the an end of the stem. The stem extension is electrically insulated from the stem. The tibial tray assembly also includes a wireless communication device configured to transmit data using the stem extension as an antenna.

Abstract: An assembly tool for assembly of a first component of a prosthesis to a second component of the prosthesis for use in joint arthroplasty. The tool includes a first member operably associated with the first component and defines a first member longitudinal axis thereof. A second member is operably associated with the second component and defines a second member longitudinal axis thereof. A washer system is coupled to the second member. A drive mechanism is coupled to washer system, such that as the drive mechanism is activated, the washer system rotates about the second member longitudinal axis and expands along the second member longitudinal axis, wherein such movement further causes the second member to move relative to the first member along the second member longitudinal axis.

Abstract: A prosthesis assembly in one embodiment includes a stem configured to be implanted in a bone and including a first coupling portion, a head having a bearing surface configured to mate with at least one of a natural opposing joint component and a prosthetic opposing joint component, the head further having a second coupling portion, a coupler including a third coupling portion and a fourth coupling portion, the third coupling portion configured to couple with the second coupling portion, and an insert including (i) a fifth coupling portion configured to couple with the fourth coupling portion in any of a plurality of rotational orientations in combination with any of a plurality of roll angles and any of a plurality of pitch angles, and (ii) a sixth coupling portion configured to couple with the first coupling portion only when the insert assumes a predetermined rotational orientation with respect to the stem.

Abstract: An orthopaedic prosthesis includes a curved outer surface configured to abut a patient's bone when the orthopaedic prosthesis is implanted therein. The outer surface may or may not be electrically conductive. A channel is defined in the outer surface and extends from a rim of the outer surface to a location on the outer surface. One or more electrical conductors is positioned in the channel and extends outwardly from the channel at the rim of the outer surface. A switch is positioned at the first location and is configured to establish an electrical connection between the electrical conductor and the outer surface and/or another electrical conductor when the first location of the outer surface contacts the patient's bone. The switch may be embodied as an end of the electrical conductor or a more complex switch such as a push-button type switch.

Abstract: An orthopaedic prosthesis includes a tibial bearing and a femoral component configured to articulate with the tibial bearing. The tibial bearing and the femoral component are configured to promote outward axial rotation of the femoral component with respect to the tibial component during knee flexion.

Abstract: A system and method for transmitting implant data includes an orthopaedic implant, a wireless receiver, and a processing circuit electrically coupled to the wireless receiver. The orthopaedic implant is configured to transmit implant identification data and implant sensor data to the wireless receiver in response to a power signal. The orthopedic implant may transfer the data over, for example, a wireless network. The processing circuit receives the implant identification data and the implant sensor data from the wireless receiver and is configured to retrieve patient-related data from a database based on the implant identification data. The processing circuit may also be configured to update a patient queue, assign a patient room to a patient, and/or transmit the patient-related data and the implant sensor data to a client machine located in the patient room.

Abstract: A method for providing joint arthroplasty includes providing a gauge for making a measurement of the contour of a long bone, making a measurement of the contour of a long bone with the gauge, providing a plurality of joint prostheses, selecting one of the plurality of joint prostheses based upon the measurement of the contour, resecting a long bone, and implanting the selected one prosthesis onto the long bone. A kit is also provided for selecting one of a plurality of joint implants for use in joint arthroplasty on a bone. The kit includes a first gauge and a second gauge.

Abstract: A method and system for registering a bone of a patient with a computer assisted orthopaedic surgery system includes retrieving an image of the bone having indicia of the position of a magnetic source coupled thereto, determining first data indicative of the position of the magnetic source in a bone coordinate system, determining second data indicative of a correlation between a coordinate system of the image and the bone coordinate system based on the first data; and displaying an image of the bone based on the second data.

Abstract: An implantable article including a biocompatible substrate and a bioactive strontium-substituted calcium phosphate ceramic apatite coating chemically bonded to at least a portion of the surface of the biocompatible substrate, wherein the strontium-substituted calcium phosphate ceramic apatite coating includes nanopores, nanocrystals and strontium ions, and includes a hexagonal crystal structure of apatite having a molar ratio of strontium ions to calcium ions of about 0.0001 to about 0.5, and the strontium ions inhibit bone resorption in vitro and enhance bone formation in vivo so that the implantable article exhibits enhance fixation and bone ingrowth in and around the implantable article.

Abstract: The present invention concerns articles having an outer surface that bears at least two layers of metal particles, wherein the at least two layers comprise an outermost layer and an intermediate layer; the outermost layer consisting essentially of aspherical metallic particles having a mean particle size of 50 to 500 microns; and the intermediate layer consisting essentially of substantially spherical metallic particles having a mean particle size of from 50 to 500 microns. In some embodiments, the outer surface has a volume porosity of between about 20% to about 80%.