ORTHOLOC(R) ADVANTIM(TM) NON-POR COAT FEMOR COMP

ORTHOLOC(R) ADVANTIM(TM) NON-POR COAT FEMOR COMP is an FDA 510(k)-cleared medical device (K930190) 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 1, 1993. Regulation: 8.