Zimmer M/L Taper Hip Prosthesis with Kinectiv Technology MR Labeling

Zimmer M/L Taper Hip Prosthesis with Kinectiv Technology MR Labeling is an FDA 510(k)-cleared medical device (K182678) 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 May 30, 2019. Regulation: 8.