AESCULAP TITANIUM BONE PLATES

AESCULAP TITANIUM BONE PLATES is an FDA 510(k)-cleared medical device (K913730) manufactured by Aesculap, 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 March 11, 1992. Regulation: 8.