MultiFIX S Ultra Knotless Fixation System

MultiFIX S Ultra Knotless Fixation System is an FDA 510(k)-cleared medical device (K153669) manufactured by Arthocare 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 January 18, 2016. Regulation: 8.