ORTHOLOC ADVANTIM L.S. TIBIAL COMPONENT

ORTHOLOC ADVANTIM L.S. TIBIAL COMPONENT is an FDA 510(k)-cleared medical device (K932911) 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 June 29, 1994. Regulation: 8.