Porous Patella

Porous Patella is an FDA 510(k)-cleared medical device (K212941) manufactured by Encore Medical, L.P. Dba Djo Surgical. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 19, 2022. Regulation: 8.