WHITESIDE ORTHOLOC M.A. TIBIAL BASE

WHITESIDE ORTHOLOC M.A. TIBIAL BASE is an FDA 510(k)-cleared medical device (K894504) 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 October 16, 1989. Regulation: 8.