An intelligent implant includes a component of an implantable prosthesis and an implantable reporting processor (IRP) associated with the implantable prosthesis. The IRP includes a housing having a casing and a cover coupled to the casing, an electronics assembly within the housing, and an antenna within the housing and coupled to the electronics assembly. The antenna is tuned to, and the electronics assembly is configured to enable communication through the antenna at both 2.45 GHZ and 403 MHZ (MICS channel). The antenna comprises a flat ribbon configured in a loop and having major surfaces. The antenna is encapsulated within the cover of the housing and is oriented therein with major surfaces of the antenna generally parallel with an inner surface of the cover.

Apparatus and methods for repairing a bone. The apparatus may include a prosthesis. The prosthesis may have a first face. The first face may be shaped to conform to a native articular bone surface and define a perimeter. The prosthesis may have a second face. The second face may be shaped to conform to a bone surface prepared for receiving the prosthesis. The second face may define two or more screw-holes adjacent the perimeter. The prosthesis may define, other than the screw-holes, no anchor pass-through.

An interbody implant to be introduced into a variety of target sites for accelerating bone ossification, for example into a space between two adjacent vertebrae. The interbody implant includes a first bone contacting surface, a second bone contacting surface, a body defined between the first and second bone contacting surfaces, and a plurality of resonators. Mechanical waves, e.g., low intensity pulsed ultrasound waves, may be transmitted to the location of the implant, causing the resonators to resonate and accelerate bone ossification.

Provided herein are hip implant devices and related surgical methods. The hip implants and methods can optionally be used in patients of Asian descent.

Provided herein is a femoral component of a hip implant device, comprising a neck having a central axis; and a body distal to the neck and having a tapered portion, wherein the body has a largest cross section perpendicular to the neck central axis, the largest cross section perpendicular to the neck central axis having a maximum height dimension and a maximum width dimension, wherein the maximum width dimension is 18.5 mm or less. The hip implant can optionally be used in patients of Asian descent.

A set of distal femoral knee prostheses which are designed to be more narrow in medial/lateral dimensions with increasing anterior/posterior size than existing prostheses to more closely correspond to the physical anatomy of female patients. The prostheses are designed to have a substantially trapezoidal shape or profile when viewed distally which features a more pronounced narrowing of the medial/lateral dimensions beginning at the posterior end of the prostheses and progressing anteriorly to the anterior end of the prostheses. Additionally, the prostheses each include a reduced profile patellar sulcus and reduced profile anterior condyles to more closely conform to the anatomy of a resected femur, and also include sulcus tracking optimized to conform to female anatomy.

A surgical implant with recesses adapted to capture fixation medium that extravasates during implantation. The implant includes an elongated stem having a distal tip configured for insertion into an implant receiving area of a patient. A collar having recesses for capturing extravasating fixation medium is attached on the stem. The collar can be fixed to the stem by a separable collar-engagement feature or the collar can be fixed to the stem via structures on the stem.

A set of distal femoral knee prostheses which are designed to be more narrow in medial/lateral dimensions with increasing anterior/posterior size than existing prostheses to more closely correspond to the physical anatomy of female patients. The prostheses are designed to have a substantially trapezoidal shape or profile when viewed distally which features a more pronounced narrowing of the medial/lateral dimensions beginning at the posterior end of the prostheses and progressing anteriorly to the anterior end of the prostheses. Additionally, the prostheses each include a reduced profile patellar sulcus and reduced profile anterior condyles to more closely conform to the anatomy of a resected femur, and also include sulcus tracking optimized to conform to female anatomy.

A method of implanting a shoulder prosthesis assembly is provided where the method includes advancing by rotation a base member, that includes a cylindrical member and a helical structure, into a resection face of a humerus of a patient such that the helical structure is submerged in and engages cancellous bone of and does not extend distally of an epiphysis of the humerus, the cylindrical member being accessible at the resection face of the humerus when the base member is so advanced; advancing a locking device into the base member until at least one elongate member spans a space between adjacent portions of the helical structure to contact the cancellous bone in the space; and inserting a retention portion of a reverse articular insert into the cylindrical member of the base member to directly connect the reverse articular insert with the cylindrical member of the base member.

Embodiments provide a method for determining an alternating magnetic field (AMF) transmitter design that produces a magnetic field that achieves a more uniform surface current or heating of an implant. Embodiments may utilize the method to be applicable to different geometries of implants and AMF transmitters. Embodiments produce a non-uniform magnetic field that in turn produces a more uniform current density/distribution on the implant surface. This leads to uniform heating and consistent biofilm reduction, while minimizing damage to adjacent tissues. Also, the differences in electrical properties such as conductivity, permittivity, and permeability of the implant components can be factored into the design process to achieve a uniform current density/distribution across components. An ultimate benefit derived from embodiments described herein is consistent biofilm reduction, inactivation, eradication, destruction, and/or removal and improved safety arising from heat conduction into surrounding tissues.