ENDO GIA REINFORCED RELOAD WITH TRI-STAPLE TECHNOLOGY

ENDO GIA REINFORCED RELOAD WITH TRI-STAPLE TECHNOLOGY is an FDA 510(k)-cleared medical device (K133938) manufactured by Covidien. 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 January 21, 2014. Regulation: 8.