
Zimmer, Inc.
Free shipping on orders over $99 · 30-day returns
MG II TOTAL KNEE SYSTEM STEMMED TIBIAL BASEPLATE COMPONENTS is an FDA 510(k)-cleared medical device (K050723) 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 April 19, 2005. Regulation: 8.