CUP, ACETABULAR, LONG POSTERIOR WALL

CUP, ACETABULAR, LONG POSTERIOR WALL is an FDA 510(k)-cleared medical device (K780398) 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 March 20, 1978. Regulation: 8.