A61F2002/30805

Prosthetic joint

A prosthetic joint (100) comprises a first component (110) having a first interface portion (111). The prosthetic joint (100) further comprises a second component (120) having a second interface portion (121) with a textured surface (122) to interface with the first interface portion (111) and form a skeletal joint. The textured surface (122) can include a plurality of concave features (123). Each or the concave features (123) can be configured to compress a lubricant (140) to facilitate hydrodynamic lubrication between the first and second interface portions (111, 121) to minimize wear between the first interface portion (111) and the second interface portion (121) of the prosthetic joint (100).

System and method for preparing bone

A method includes generating a surgical plan for installation of a structure at a bone and controlling a controllable guide structure to guide a cutting tool to sculpt the bone and the structure based on the surgical plan. Sculpting the bone provides the bone with a bone mating surface and sculpting the structure provides the structure with a structure mating surface. The method also includes installing the structure on the bone by engaging the structure mating surface of the structure with the bone mating surface of the bone.

Artificial vertebral endplates and associated methods

In a general aspect, an apparatus can include a plate configured for implantation in a body of a patient. The plate can include a plurality of pores and be configured for placement between a cancellous bone of a spinal vertebra and a corresponding cartilaginous endplate as a replacement for a bony endplate of the spinal vertebra.

Engineered Sterile Cartilage Implant Plug(s) With Sterile, Specific Instrument Kit(s)
20240398583 · 2024-12-05 · ·

An apparatus and a method are provided for performing cartilage graft implant surgeries. The apparatus comprises a graft plug kit comprising one or more grafts configured to treat osteochondral defects in various bone joint locations in a patient's body. Each of the grafts comprises a cartilage layer coupled with a bone portion. The cartilage layer comprises a thickness selected to closely match the thickness of existing cartilage at an implant location. The bone portion comprises surface features configured to encourage the patient's bone tissue to grow into the bone portion, thereby accelerating incorporation of the graft into the patient's bone. An instrument kit comprises a multiplicity of instruments configured for implantation of the grafts into the patient's body, including at least a graft inserter, a guidewire, a reamer, and a size gauge.

Implant with multi-layer bone interfacing lattice

An implant includes a body including a substrate and a bone interfacing lattice disposed on the substrate. The bone interfacing lattice includes at least two layers of elongate curved structural members. In addition, the at least two layers of elongate curved structural members include a first layer adjacent the substrate and a second layer adjacent the first layer. Also, the first layer has a first deformability and the second layer has a second deformability, wherein the second deformability is greater than the first deformability. Further, one or more of the elongate curved structural members may have a spiraling geometry.

Femoral stem with partially recessed porous coating

The femoral stem prosthesis includes a prosthesis body having a neck, stem, and porous coating receiving area. A portion of a transition between the porous coating receiving area and the stem is defined by a recess where the porous coating receiving area inwardly extends by a depth relative to the stem while the porous coating receiving area is approximately flush with the stem about a remainder of the transition between the porous coating receiving area and the stem. A porous coating overlying the porous coating receiving area has a thickness approximately equal to the depth of the recess to define a smooth transition between the porous coating and the stem along the portion of the transition by the at least one recess and a collar outwardly extending relative to the stem by approximately the thickness along the remainder of the transition between the porous coating receiving area and the stem.

Spline oriented indexing guide
09622759 · 2017-04-18 · ·

A surgical cutting system can be configured to prepare an intervertebral space for insertion of an intervertebral implant. In an embodiment, the surgical cutting system includes a drill guide and a drill bit. The drill guide can be configured to be coupled to a trial implant and can include a guide portion that is configured to support a first stop member. In addition, the drill guide defines a guide hole that extends through the guide portion along a guide hole axis. The drill bit can be configured to be at least partially received in the guide hole. Moreover, the drill bit defines a second stop member that is configured abut the first stop member so as to limit movement of the drill bit through the guide hole along the guide hole axis to a maximum cut depth.

FEMORAL STEM WITH PARTIALLY RECESSED POROUS COATING
20170056184 · 2017-03-02 ·

The femoral stem prosthesis includes a prosthesis body having a neck, stem, and porous coating receiving area. A portion of a transition between the porous coating receiving area and the stem is defined by a recess where the porous coating receiving area inwardly extends by a depth relative to the stem while the porous coating receiving area is approximately flush with the stem about a remainder of the transition between the porous coating receiving area and the stem. A porous coating overlying the porous coating receiving area has a thickness approximately equal to the depth of the recess to define a smooth transition between the porous coating and the stem along the portion of the transition by the at least one recess and a collar outwardly extending relative to the stem by approximately the thickness along the remainder of the transition between the porous coating receiving area and the stem.

Sleeve augment device for an articulated joint

An augment device for a joint endoprosthesis, the device comprising: a sleeve having a top and a bottom, a distance between said top and said bottom defining an entire height of said sleeve, wherein the sleeve surrounds a channel extending through the sleeve from the top to the bottom of the sleeve wherein the channel is configured to receive a stem of the joint endoprosthesis; the sleeve comprising an inner face and an outer face, the inner face defining the channel, and a distance between the inner face and the outer face defining a thickness; the sleeve further comprising a porous material configured for ingrowth of bony material.

SYSTEM AND METHOD FOR PREPARING BONE

A method includes generating a surgical plan for aligning a structure with a first bone segment and a second bone segment, and controlling a controllable guide structure to guide a cutting tool to sculpt the first bone segment, the second bone segment, and the structure based on the surgical plan. The method can include providing the first bone segment with a first bone mating surface by sculpting the first bone segment, providing the second bone segment with a second bone mating surface by sculpting the second bone segment, and providing, by sculpting the structure, the structure with at least one structure mating surface that is complementary to at least one of the first bone mating surface or the second bone mating surface.