Stryker All-PEEK Knotless Anchor System

Stryker All-PEEK Knotless Anchor System is an FDA 510(k)-cleared medical device (K181083) manufactured by Stryker. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 22, 2018. Regulation: 8.