PERIARTICULAR LOCKING PLATES AND SCREWS, 2357 AND 2359 SERIES

PERIARTICULAR LOCKING PLATES AND SCREWS, 2357 AND 2359 SERIES is an FDA 510(k)-cleared medical device (K042598) manufactured by Zimmer, 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 October 28, 2004. Regulation: 8.