RENOVIS SURGICAL POROUS ACETABULAR CUP SYSTEM

RENOVIS SURGICAL POROUS ACETABULAR CUP SYSTEM is an FDA 510(k)-cleared medical device (K141676) manufactured by Renovis Surgical Technologies, 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 November 3, 2014. Regulation: 8.