Ethicon Circular Stapler, Ethicon Circular Stapler -XL Sealed

Ethicon Circular Stapler, Ethicon Circular Stapler -XL Sealed is an FDA 510(k)-cleared medical device (K201280) manufactured by Ethicon Endo-Surgery, LLC. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 26, 2020. Regulation: 8.