ZMR HIP SYSTEM-REVISION TAPER

ZMR HIP SYSTEM-REVISION TAPER is an FDA 510(k)-cleared medical device (K992667) 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 October 26, 1999. Regulation: 8.