WHITESIDE ORTHOLOC MODULAR TIBIAL CONSTRAIN.INSERT

WHITESIDE ORTHOLOC MODULAR TIBIAL CONSTRAIN.INSERT is an FDA 510(k)-cleared medical device (K905076) 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 12, 1991. Regulation: 8.