DePuy Actis Duofox Hip Prosthesis

DePuy Actis Duofox Hip Prosthesis is an FDA 510(k)-cleared medical device (K150862) manufactured by DePuy Orthopaedics, 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 September 24, 2015. Regulation: 8.