Argo Knotless GENESYS Anchor

Argo Knotless GENESYS Anchor is an FDA 510(k)-cleared medical device (K244025) manufactured by Conmed 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 27, 2025. Regulation: 8.