
Zimmer, Inc.
Free shipping on orders over $99 · 30-day returns
Persona® Revision Knee System (Persona Revision SoluTion Femoral Components) is an FDA 510(k)-cleared medical device (K243724) manufactured by Zimmer, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 5, 2025. Regulation: 8.

Synthes (Usa)
SKU K100676
BackorderedMedline
SKU VM-1270020

Cardinal Health
SKU VM-1270026
BackorderedMoog
SKU VM-1270057