ORTHOLOC(R) ADVANTIM(TM) POSTERIOR STAB FEMOR COMP

ORTHOLOC(R) ADVANTIM(TM) POSTERIOR STAB FEMOR COMP is an FDA 510(k)-cleared medical device (K930189) 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 August 5, 1993. Regulation: 8.