RESTORIS MCK PatelloFemoral Component - Patellofemoral joint prosthesis

Country: Australia

Language: English

Source: Department of Health (Therapeutic Goods Administration)

Available from:

Stryker Australia Pty Ltd

Class:

Class III

Manufactured by:

MAKO Surgical Corp 3365 Enterprise Avenue, Weston, Florida, 33331 United States Of America

Therapeutic area:

58227 - Patellofemoral joint prosthesis

Therapeutic indications:

A sterile implantable Patellofemoral component of the RESTORIS? MCK (MultiCompartmental Knee) made of Cobalt chromium (CoCr), designed to articulate with an artificial Patella component. For cemented use only. A femoral implant used in cemented patellofemoral arthroplasty in patients with degenerative arthritis in the distal femur and patella, patients with a history of patellar dislocation or patella fracture, or patients with failed previous surgery (arthroscopy, tibial tubercle elevation, lateral release) where pain, deformity or dysfunction persists. Or for single or multi-compartmental knee replacement when used in conjunction with the RIO, Robotic arm Interactic Orthopaedic system.

Authorization status:

A

Authorization date:

2015-06-12