LEGION CR Porous Plus HA Femoral Components

LEGION CR Porous Plus HA Femoral Components is an FDA 510(k)-cleared medical device (K211246) manufactured by Smith & Nephew, 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 May 23, 2021. Regulation: 8.