MultiFIX® P Knotless Fixation Device

MultiFIX® P Knotless Fixation Device is an FDA 510(k)-cleared medical device (K151897) manufactured by ArthroCare Corporation. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 5, 2015. Regulation: 8.