Arthrex Radiopaque FiberTape Cerclage sutures

Arthrex Radiopaque FiberTape Cerclage sutures is an FDA 510(k)-cleared medical device (K230976) manufactured by Arthrex, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 23, 2023. Regulation: 8.