MODIFIED ENDO STICH

MODIFIED ENDO STICH is an FDA 510(k)-cleared medical device (K082659) manufactured by Covidien Lp, Formerly Registered AS United States. 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 September 18, 2008. Regulation: 8.