OMNI ARC Anteverted Neck Hip Stem

OMNI ARC Anteverted Neck Hip Stem is an FDA 510(k)-cleared medical device (K172467) manufactured by Omnilife Science. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 20, 2017. Regulation: 8.