AlphaVent Knotless SP PEEK Anchor

AlphaVent Knotless SP PEEK Anchor is an FDA 510(k)-cleared medical device (K233893) 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 January 24, 2024. Regulation: 8.