ANATOMIC MODULAR KNEE (AMK) POSTERIOR STABILIZED

ANATOMIC MODULAR KNEE (AMK) POSTERIOR STABILIZED is an FDA 510(k)-cleared medical device (K901406) manufactured by Depuy, 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 July 22, 1990. Regulation: 8.