FOUNDATION POROUS ACETABULAR SYSTEM

FOUNDATION POROUS ACETABULAR SYSTEM is an FDA 510(k)-cleared medical device (K973119) manufactured by Encore Orthopedics, 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 27, 1998. Regulation: 8.