Abstract: A method of performing a computer-assisted orthopaedic procedure includes securing a sensor support instrument to the patient's bone. A number of sensors are secured to the support instrument. A computer-assisted orthopaedic surgical instrument is also disclosed.

Abstract: A number of orthopaedic surgical instruments are also disclosed. A method, apparatus, and system for fabricating such instruments are also disclosed.

Abstract: A mounting bracket for use with a reference array of a computer assisted surgery system includes a base and an arcuate support frame coupled to the base. The base is configured to be secured to a bone of a patient. The arcuate support frame includes a plurality of mounts. Each mount is configured to receive a mounting end of the reference array. In some embodiments, the arcuate support frame may be pivotable with respect to the base. Additionally, in some embodiments, the arcuate support frame may be movable about an arc defined by the arcuate support frame.

Abstract: A number of orthopedic surgical instruments are also disclosed. A method, apparatus, and system for fabricating such instruments are also disclosed.

Abstract: A method and system for designing a patient-specific orthopaedic surgical instrument includes coupling a knee sleeve to a leg of the patient. The knee sleeve includes sensors configured to generate sensor data indicate of the position of the respective sensor. The method also include determining angulation data indicative of the angulation of the knee based on the sensor data. The angulation data may be indicative of, for example, the ligament laxity of the knee. The method may also include generating a medical image(s) of the knee. The design of the patient-specific orthopaedic surgical instrument is determined based on the angulation data and the medical image(s).

Abstract: The present disclosure is directed to a cleansing solution and system for administering the cleansing solution to decontaminate a wound surface. A method and kit for decontaminating a wound surface is also provided.

Abstract: Disclosed is a polymeric orthopaedic bearing material for use as an implant material or part thereof comprising one or more crosslinked regions and one or more non-crosslinked or substantially non-crosslinked regions at the surface. The bearing material can be prepared from a crosslinkable polymer, e.g., ultrahigh molecular weight polyethylene. The orthopaedic bearing material has an advantageous combination of at least one wear property and at least one mechanical property. Also disclosed are processes for producing orthopaedic bearing materials, for example, by irradiating a raw material in consolidated form through a radiation mask having a perforated pattern for crosslinking selected regions of the raw material, and optionally shaping the raw material into a bearing material. Alternatively, a pulsed radiation beam can be used for crosslinking.

Abstract: A number of orthopaedic surgical instruments are also disclosed. A method, apparatus, and system for fabricating such instruments are also disclosed.

Abstract: An implant includes a body configured to be implanted at least partially within a bone canal. The body has a proximal end, a longitudinal axis and a cavity located at the proximal end. The cavity is configured to mate with an insertion tool and defines a cavity axis that is not parallel to the longitudinal axis of the implant.

Abstract: Orthopaedic devices are disclosed. The devices include a part that is made of extracellular matrix material that has been hardened. One method of hardening the extracellular matrix is to comminute naturally occurring extracellular matrix and dry the comminuted material. The hardened extracellular matrix material can be machined to form a variety of orthopaedic devices.

Abstract: An instrument for recording and replicating the spatial orientation of a dialable component of an implant relative to a bone engaging component of the implant includes a base assembly configured to support the trial implant so that the datum is in a predetermined orientation, a fixture supported on said base assembly, said fixture including an alignment tool configured to engage the first dialable component of the trial implant when the trial implant is supported by said base assembly, and a locking assembly configured to record the angular orientation of said alignment tool relative to said fixture with said alignment tool engaged with the first dialable component, and to replicate the recorded angular orientation with the alignment tool and a second dialable component.

Abstract: A mobile tibial assembly includes a tibial tray and a unicompartmental tibial insert configured to move relative to the tibial tray. The tibial insert includes a platform having an upper bearing surface and a stem extending downwardly from a bottom surface of the unicompartmental insert. The tibial tray includes a corresponding recess, such as a cavity and/or a channel, configured to receive the stem therein such that the stem and the recess cooperate to constrain the movement of the unicompartmental tibial insert relative to the tibial tray. The stem of the unicompartmental tibial insert is configured to extend below the bottom surface of the tibial tray when received in the cavity.

Abstract: One embodiment of the present invention is directed to compositions and methods for enhancing attachment of soft tissues to a metal prosthetic device. In one embodiment a construct is provided comprising a metal implant having a porous metal region, wherein said porous region exhibits a nano-textured surface, and a biocompatible polymer matrix coating the nano-textured surface. The polymer matrix coating comprises a naturally occurring extracellular matrix with biocompatible inorganic materials distributed within the matrix, or a biocompatible polymer and an osteo-inductive agent.

Abstract: A number of orthopaedic surgical instruments are also disclosed. A method, apparatus, and system for fabricating such instruments are also disclosed.

Abstract: An implantable orthopaedic knee prosthesis includes a component that is configured to be coupled to a surgically-prepared bone. A fixation side of the component includes a fixation surface that has an angled cement pocket formed therein.

Abstract: A first articulating member for use with a second articulating member to form a prosthesis for use in joint arthroplasty for a joint formed between adjacent first and second bones in which a bone fragment having an exterior surface has separated from the first bone is provided. The first articulating member includes an articulating portion having an articulation surface for articulation with the second articulating member and an attaching portion connected to the articulating portion for attachment to the first bone. The first articulating member also includes a fragment portion connected to at least one of the articulating portion and the insertion portion. The fragment portion includes a surface for contact with the external periphery of the bone fragment.

Abstract: The invention provides a medical implant device or component thereof comprising a metal substrate, an intermediate coating, and an outer coating of aluminum oxide, as well as a method of making such a medical implant device or component thereof.

Abstract: A joint prosthesis includes a bone engaging portion having a first recess portion, and an internal wall defining a second recess portion, an articulating component, an insert component having (i) a first insert portion configured to snugly fit within said second recess portion in contact with the internal wall, and (ii) a projecting portion that fixedly projects from said first insert portion and is configured to snugly fit with the first recess portion so as to rotationally fix the first insert portion within the second recess portion, said insert component also having a first coupling portion, and a mating component configured to mate with said articulating component and having a second coupling portion configured to mate with the first coupling portion to form a fixed male/female couple at variable version and inclination angular orientations with respect to the insert component.

Abstract: A prosthetic femoral stem component includes a body element, a neck element and a stem element. The body element, neck element and stem element are secured to one another with a modular connection, the modular connection having a taper junction and an engaged-fit junction. The engaged-fit junction is formed by interaction of first and second concentric walls, the first concentric wall being formed on a shaft of the neck element and the second concentric wall being formed along a portion of a sidewall defining an aperture extending through the body element.

Abstract: The present invention relates to processes involving contacting articles that include titanium or titanium alloy with a solution comprising hydrochloric acid and chloride-containing compound for a time and at a temperature effective to form a plurality of indentions that, independently, have a diameter of from about 200 nm to 10 microns.