Zimmer® Persona® Personalized Knee System

Zimmer® Persona® Personalized Knee System is an FDA 510(k)-cleared medical device (K243293) manufactured by Zimmer Biomet. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 19, 2024. Regulation: 8.