Metal/composite hybrid orthopedic implants

Claim 2

An orthopedic device adapted for implantation within a body, the device comprising: an intraosseous metal portion; and an intraosseous composite portion of one or more layers and comprising (i) a first extension having a modulus and that is received within said metal portion and secured thereto and (ii) a second extension positioned outside said metal portion; said composite portion having a length and comprising one or more filaments disposed about a longitudinal axis by winding or braiding each filament along said length at winding or braiding angles with respect to the longitudinal axis selected to provide the second extension with a modulus that is less than the modulus of the first extension, the winding or braiding angle in some of the layers of the first extension being less than the winding or braiding angle in the same layers of the second extension, said filaments further being disposed within a polymer matrix.

Claim 3

The orthopedic device of claim 1 wherein the cross-sectional area of said first extension is different from the cross-sectional area of said second extension.

Claim 4

The orthopedic device of claim 1 wherein said first and second extensions are cylindrical.

Claim 5

The orthopedic device of claim 1 wherein said first extension forms a taper such that the cross-sectional area of said extension decreases proximally.

Claim 6

The orthopedic device of claim 4 wherein the maximum cross-sectional area of said first extension is different from the cross-sectional area of said second extension, said extensions being joined by a bevelled transition portion having a cross-sectional area equal to that of said first extension at the first extension-bevelled portion interface and a cross-sectional area equal to that of said second extension at the second extension-bevelled portion interface.

Claim 7

An orthopedic device adapted for implantation within a body, the device comprising: an intraosseous metal portion; an intraosseous composite portion of one or more layers and comprising a first extension having a modulus and that is received within said metal position and secured thereto and a second extension positioned outside said metal portion; and an intraosseous metal insert interposed there between and connecting said metal portion to said composite portion, said metal insert being received within said metal portion and frictionally secured thereto, said metal insert further forming a taper such that the cross-sectional area of said metal insert increases from a first end received within said metal portion and a second end connected to said composite portion, said metal insert further being connected to said composite portion by an adhesive joint or a shrink fit joint, said composite portion having a length and comprising one or more filaments disposed about a longitudinal axis by winding or braiding the filaments at winding or braiding angles with respect to the longitudinal axis selected to provide the second extension with a modulus that is less than the modulus of the first extension the winding or braiding angles in some of the layers of the first extension being less than the winding or braiding angle in the same layers of the second extension, said filaments further being disposed within a polymer matrix; and said intraosseous metal portion and said intraosseous composite portion adapted to contact the body.

Claim 8

An orthopedic device adapted for implantation within a body, the device comprising: an intraosseous metal portion; an intraosseous composite portion of one or more layers and comprising a first extension having a modulus and that is received within said metal position and secured thereto and a second extension positioned outside said metal portion; and an intraosseous metal insert interposed there between and connecting said metal portion to said composite portion, said metal insert being received within said metal portion and frictionally secured thereto, said metal insert further forming a taper such that the cross-sectional area of said metal insert increases from a first end received within said metal portion and a second end connected to said composite portion, said metal insert further being connected to said composite portion by an adhesive joint or a shrink fit joint, said composite portion having a length and comprising one or more filaments disposed about a longitudinal axis by winding or braiding the filaments at winding or braiding angles with respect to the longitudinal axis selected to provide the second extension with a modulus that is less than the modulus of the first extension the winding or braiding angles in some of the layers of the first extension being less than the winding or braiding angle in the same layers of the second extension, said filaments further being disposed within a polymer matrix; and said intraosseous metal portion and said intraosseous composite portion adapted to contact the body.

Claim 9

The orthopedic device of claim 1 wherein the intraosseous metal portion is selected from the group consisting essentially of stainless steel, cobalt-chrome alloy, and titanium alloy.

Claim 10

The orthopedic device of claim 1 wherein the polymer matrix is selected from the group consisting essentially of polysulfone, polyether-ether-ketone, polyether-ketone-ketone, polyimide, epoxy, and polycyanate.

Claim 11

The orthopedic device of claim 1 wherein the filaments are selected from the group consisting essentially of carbon, graphite, glass, and aramid fiber.

Claim 12

The orthopedic device of claim 1 useful as a human hip implant wherein the intraosseous metal portion is a proximal metal body and the intraosseous composite portion is a distal composite stem.

Claim 13

The orthopedic device as defined in claim 1, said second extension having an equivalent flexural modulus, E c , selected according to the criteria: E.sub.c <E.sub.1 where σ.sub.b /σ.sub.b "=1 when E.sub.c =E.sub.1 and E.sub.c >E.sub.2 where S/S"=1 when E.sub.c =E.sub.2 wherein σ b is the maximum bending stress in the bone adjacent to the implanted device at the extension of the composite portion positioned outside of the metal portion; σ b " is the maximum bending stress in the bone adjacent to the implanted orthopedic device wherein the intraosseous portion is entirely metal affixed in place by polymethylmethacrylate bone cement; S is the rotatory stiffness of the implanted device including the composite portion and the metal portion; and S" is the rotatory stiffness of the implanted device of metal affixed with bone cement.

Claim 14

The orthopedic device as defined in claim 1, said composite portion having an equivalent flexural modulus of up to 16 million psi.

Claim 15

The orthopedic device as defined in claim 1, wherein the second extension has an equivalent flexural modulus of 1 million to 8 million psi.