WHITESIDE BIOMECHANICS CANCELLOUS BONE SCREW

WHITESIDE BIOMECHANICS CANCELLOUS BONE SCREW is an FDA 510(k)-cleared medical device (K961157) manufactured by Whiteside Biomechanics, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 16, 1996. Regulation: 8.