SCREW, WADSWORTH OLECRANON

SCREW, WADSWORTH OLECRANON is an FDA 510(k)-cleared medical device (K770035) manufactured by Orthopedic Equipment Co., 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 January 13, 1977. Regulation: 8.