Knotilus+ PEEK Knotless Anchor

Knotilus+ PEEK Knotless Anchor is an FDA 510(k)-cleared medical device (K232683) manufactured by Stryker Endoscopy. 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 23, 2023. Regulation: 8.