ORTHOLOC ADVANTIM TIBIAL BASE COMPONENT

ORTHOLOC ADVANTIM TIBIAL BASE COMPONENT is an FDA 510(k)-cleared medical device (K932858) 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 February 15, 1994. Regulation: 8.