ORTHOLOC ADVANTIM REVISION FEMORAL COMPONENT

ORTHOLOC ADVANTIM REVISION FEMORAL COMPONENT is an FDA 510(k)-cleared medical device (K932210) manufactured by Dow Corning Wright. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 6, 1994. Regulation: 8.