SpeedLock Knotless Fixation System

SpeedLock Knotless Fixation System is an FDA 510(k)-cleared medical device (K153313) 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 December 10, 2015. Regulation: 8.