DURACON INSET PATELLA WITH CENTRAL PEG

DURACON INSET PATELLA WITH CENTRAL PEG is an FDA 510(k)-cleared medical device (K961482) manufactured by Howmedica Corp.. 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 4, 1996. Regulation: 8.