WHITESIDE ORTHOLOC II REV POST STAB TOTAL KNEE SY

WHITESIDE ORTHOLOC II REV POST STAB TOTAL KNEE SY is an FDA 510(k)-cleared medical device (K871776) 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 2, 1987. Regulation: 8.