MG II POROUS TOTAL KNEE SYSTEM

MG II POROUS TOTAL KNEE SYSTEM is an FDA 510(k)-cleared medical device (K892800) 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 August 2, 1989. Regulation: 8.