MODIFICATION OF DEPUY ACE TIMAX MEDIAL PILON PLATE

MODIFICATION OF DEPUY ACE TIMAX MEDIAL PILON PLATE is an FDA 510(k)-cleared medical device (K990120) 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 January 31, 1999. Regulation: 8.