DEPUY ACE TIMAX CALCANEAL PERI-ARTICULAR PLATE

DEPUY ACE TIMAX CALCANEAL PERI-ARTICULAR PLATE is an FDA 510(k)-cleared medical device (K981775) manufactured by Depuy Ace Medical Co.. 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 28, 1998. Regulation: 8.