AGC V2 Total Knee Anatomic Porous Posterior Stabilised Femoral Component - Posterior-stabilized total knee prosthesis

País: Austrália

Língua: inglês

Origem: Department of Health (Therapeutic Goods Administration)

Disponível em:

Zimmer Biomet Pty Ltd

Classe:

Class III

Fabricado por:

Biomet UK Ltd Waterton Industrial Estate, Bridgend, South Glamorgan, CF31 3XA United Kingdom

Área terapêutica:

33665 - Posterior-stabilized total knee prosthesis

Indicações terapêuticas:

Titanium porous coated chrome cobalt cruciate substituting femoral knee component with deep patella track, wide femoral condyles Porous coated chrome cobalt femoral component for cementless use in AGC V2 Total Knee arthroplasty when the cruciate ligament requires substitution; to provide a means of reducing pain and restoring function. The indications for use include: Osteoarthritis, rheumatoid arthritis; Traumatic arthritis; Failure of a previous joint replacement procedure; Correction of varus, valgus or post-traumatic deformity; Correction or revision of unsuccessful osteotomy or arthrodesis.

Status de autorização:

Included