ENDO GIA RELOAD

ENDO GIA RELOAD is an FDA 510(k)-cleared medical device (K130717) manufactured by Covidien, Formerly US Surgical A Divison of Tyco H. 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 April 17, 2013. Regulation: 8.