Tornier Sas

Integra Lifesciences Corporation

Irene Ferrari

Yves-Alain Ratron

Pascal Boileau

Gilles Walch

Lucile Ferrand

Michael Weber

A method of forming a shoulder prosthesis includes resecting an end portion of a humerus to form a resected end of the humerus and a resected portion separated from the humerus, the resected portion having an outer convex surface and an inner surface. The inner surface of the resected portion is processed to include a concave articular surface. The outer convex surface of the resected portion is implanted in the resected end of the humerus. An implant having a convex articular surface is secured to a glenoid. The concave articular surface of the resected portion is articulated with the convex articular surface of the implant.

Intra-articular joint replacement

A prosthetic ankle assembly including an astragalar component with an upper articular surface that forms part of an ankle joint prosthesis and a lower surface with a shape adapted to engage an upper face of an astragalus. An astragalocalcanean rod is positioned in an astragalocalcanean channel extending from the lower face of the calcaneus to the upper surface of the astragalus. A first end of the astragalocalcanean rod is engage with the lower surface of the astragalar component and a second end of the astragalocalcanean rod is engaged with a lower region of the calcaneus. A distance between the second end of the astragalocalcanean rod is adjustable relative to the lower surface of the astragalar component to adjustably compress the calcaneus against the astragalus.

Ankle prosthesis for the arthrodesis of the calcaneum

A method of forming a shoulder prosthesis includes forming a concave articular surface into an end portion of a humerus, including compacting bone of the end portion to define the concave articular surface. An implant having a convex articular surface is secured to a glenoid. The concave articular surface of the humerus is articulated with the convex articular surface of the implant.

A glenoid component for a shoulder prosthesis adapted to be mounted in a glenoid cavity of a shoulder. An elongated keel adapted to engage with the glenoid cavity is attached to the internal surface of the base. The keel extends along a longitudinal axis of the base. The keel includes various configurations of transverse members extending away from the longitudinal axis. The surgeon selects a glenoid component with a keel and transverse member configuration that is anatomically optimized for the patient. Glenoid components properly optimized provide mechanical strength and stability superior to prior art devices. The glenoid components disclosed herein are particularly well suited for use in an anatomical total shoulder prosthesis, but may are also suited to partial shoulder prostheses and reverse shoulder prostheses.

Growing community of inventors

Le Touvet, France

Irene Ferrari