Zimmer Knee Joint Replacement Prostheses MR Labeling

Zimmer Knee Joint Replacement Prostheses MR Labeling is an FDA 510(k)-cleared medical device (K173057) 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 March 28, 2018. Regulation: 8.