ICONN Revolution Knotless Suture Anchor

ICONN Revolution Knotless Suture Anchor is an FDA 510(k)-cleared medical device (K182264) manufactured by Iconn Orthopedics, LLC. 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 18, 2018. Regulation: 8.