Abstract: A method and apparatus for obtaining various components of a multi-component material. Generally, a component of a whole blood sample may be concentrated from a patient and re-introduced to the same patient. For example, a clotting component, such as thrombin, from a whole blood sample may be extracted and concentrated in an apparatus and collection to be reapplied or reintroduced into a patient.

Abstract: A prosthesis includes an implant defining an attachment surface thereon. A porous insert is selectively coupled to the implant. The porous insert is adapted to be received at the attachment surface of the implant in a retained position. The porous insert is adapted to facilitate tissue ingrowth. In one embodiment the implant comprises a femoral component. The femoral component comprises an inner condylar portion having a first and second lateral sidewalls, an anterior wall and a posterior wall defining a box. The box defines the attachment surface. In other embodiments, the implant comprises a hip stem and an acetabular shell.

Abstract: An orthopedic prosthesis for implantation into a bone of a patient includes a porous metal shell adapted to be affixed within the bone. The porous metal shell includes an outer surface adapted to receive bone ingrowth and an inner surface adapted to engage a liner. The porous metal shell is porous from the outer surface to the inner surface. A non-porous member may be affixed to the porous metal shell. The non-porous member may include a piercing member extending from the outer surface, the piercing member adapted to penetrate the bone in an implanted position. The non-porous member may include spikes or fins. In one example, the piercing member may define a reduced material cross section at an interface with the outer surface of the porous metal shell. The piercing member may be adapted to be broken at the reduced material cross section and removed from the porous metal shell.

Abstract: A constraining prosthesis to reduce the possibility of a dislocation of the prosthesis after implantation is taught. A constraining liner is taught to include a constraining passage smaller than an internal diameter of the liner. A head can include a portion that is small enough to be positioned into the liner. The head can include a second dimension that is greater than the opening to constrain the modular head within the liner. A kit is also taught for trialing prosthesis to provide and determine a customized and personal fit of the prosthesis for each patient.

Abstract: A method and apparatus for separation, concentration, and/or applying a biological or bio-engineered fluid. Generally, the fluid application device includes a sprayer body to enable the application of the fluid and a container adaptable to enable the separation of the fluid into at least a first component and a second component. The container is releasably coupled to the nozzle. The nozzle is adapted to withdraw at least one of the first component or the second component from the container after the fluid has been separated to apply the fluid to a selected site.

Abstract: A method for forming an acetabular shell includes providing a working surface such as a mandrel, and spraying the working surface with a first layer of material having a first composition such as aluminum oxide. After a suitable thickness is generated, the spray composition is gradually changed to other compositions having desired particle sizes and distribution. In one example, the composition is changed to a mixture of aluminum oxide and titanium oxide and/or titanium. As thickness builds up, the relative amount of aluminum oxide is decreased such that the composition is all titanium and titanium oxide. After a desired thickness is generated, the acetabular shell is extracted off the mandrel.

Abstract: A method and apparatus for replacing a selected portion of the anatomy is described. In particular, a prosthesis can be provided to replace a portion of an articulating joint, such as an elbow. The apparatus can be modular for various reasons and each of the modular portions can include a different dimension to achieve a selected result. For example, the prosthesis can achieve a different size condylar replacement, a selected offset, a selected articulation, or combinations thereof.

Abstract: A prosthetic system for replacement of a portion of a hip bone including a plurality of acetabular components and a plurality of flange components. The prosthetic system also includes a plurality of pubis components. Each of the pubis components and each of the flange components are operable to connect to each of the acetabular components. Each of the pubis components define a clamping portion that is configured to attach to an opposed healthy pubis bone. An angle between the flange component and the pubis component varies among the acetabular components.

Abstract: A pelvic implant assembly and associated methods. The implant assembly includes an acetabular component, and a compliant fixator coupling the acetabular component to the pelvis.

Abstract: A prosthesis includes a trunnion having a first end defining a uniform cross-section and a second end adapted to be fixed to a prosthesis stem. A ceramic head has a first bearing surface on which a second prosthesis fixed to a second bone can articulate. The ceramic head defines a recess. The first end of the trunnion is fixedly received within the recess. The second end of the trunnion is releasably connectable to the prosthesis stem by a taper connection.

Abstract: A guide for cutting a bone comprising an anterior portion and a distal portion orientated at about a right angle to the anterior portion. The distal portion includes a guiding side, a distal surface at the guiding side, a box-cut shaped opening defined by the guiding side, a plurality of first cutting surfaces disposed at the guiding side at an acute angle relative to the distal surface of the guiding side operable to guide a cutting device to the bone to form chamfer cuts in the bone, and a second cutting surface disposed at the guiding side at at least about a right angle to the distal surface operable to guide a cutting device to the bone to form a posterior cut in the bone.

Abstract: A resurfacing implant comprising a head and an extended articulating surface protruding from a portion of the head operable to articulate with at least one of a bone and a ligament. The head has an exterior articulating surface, an interior surface opposite the exterior articulating surface, and an anchoring device extending from the interior surface.

Abstract: An implant assembly and associated method for selectively performing reverse and traditional arthroplasty for a shoulder joint that includes a humerus and a glenoid. The implant assembly may include a head, a cup, a humeral stem and an adaptor. The method includes inserting the humeral stem to the humerus and connecting a male taper of the adaptor to a female taper of the head. For reverse arthroplasty, the method includes attaching the adaptor to the glenoid and the cup to the stem. For traditional arthroplasty, the method includes attaching the adaptor to the humeral stem and the cup to the glenoid. The method also includes articulating the head with the cup.

Abstract: A knee prosthetic for implantation includes a mobile rotatable posterior stabilized (PS) post. The mobile PS post may rotate or distract superiorly relative to a tibial component. The mobile PS post may rotate with the femur after implantation, at least for a selected distance. Various exterior shapes of the mobile PS post and/or a bore formed in the tibial component may be selected to limit the amount of rotation. Various materials may be chosen to form the mobile PS post depending upon desired qualities.

Abstract: A two piece humeral component for use in joint arthroplasty which is adapted to be implanted into a joint and engaged by a socket component of the joint. The joint component includes a body having a first articulating surface and a second medial surface opposite the first articulating surface. The first articulating surface is adapted to be engaged by the socket and the second medial surface is adapted to be secured to mounting portion. The mounting portion has a first surface and a second medial surface. The first surface is adapted to be fixably engaged to the second mounting portion of the humeral component. The second medial surface is adapted to be secured to the humerus. A peg which has a first end adapted to engage a cavity found in the humerus is disposed on the mounting portion's second medial surface.

Abstract: A biological therapeutic delivery device is provided. In one preferred embodiment, the invention includes a device for effectuating localized tissue injury comprised of a resorbable body having at least one therapeutic agent and a retention device to anchor the agent within a tissue, the therapeutic agent being released into the tissue as the body resorbs. In an additional preferred embodiment, the invention includes a device for effectuating localized tissue injury comprised of a resorbable body having a cavity containing a therapeutic agent and a series of projections extending from the body to anchor the body in a tissue, the therapeutic agent being released into the tissue as the body resorbs.

Abstract: A modular prostheses system for replacement of the radial head portion of the radius bone, and methods for its use are disclosed. The system comprises a stem component comprising a anchoring portion and a mounting portion, and a head component having an open channel wherein the open channel is configured to connect to the mounting portion along an assembly axis that is transverse to a longitudinal axis of the stem component.