BASX BLADELESS TROCAR

BASX BLADELESS TROCAR is an FDA 510(k)-cleared medical device (K062209) manufactured by Ethicon Endo-Surgery, LLC. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 9, 2006. Regulation: 8.