ETHICON ENDO-SURGERY GENERATOR G11, MODEL GEN11

ETHICON ENDO-SURGERY GENERATOR G11, MODEL GEN11 is an FDA 510(k)-cleared medical device (K101990) manufactured by Ethicon Endo-Sugery, 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 June 12, 2011. Regulation: 8.