ARC-2F ACETABULAR CUP

ARC-2F ACETABULAR CUP is an FDA 510(k)-cleared medical device (K893785) manufactured by Protek, 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 August 8, 1989. Regulation: 8.