MPF ACETABULAR CUP GENERATION 2

MPF ACETABULAR CUP GENERATION 2 is an FDA 510(k)-cleared medical device (K022120) manufactured by Plus Orthopedics. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 23, 2002. Regulation: 8.