HARMONIC SCALLOP BLADE, GENERATOR G11

HARMONIC SCALLOP BLADE, GENERATOR G11 is an FDA 510(k)-cleared medical device (K141122) manufactured by Ethicon Endo-Surgery, 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 September 14, 2014. Regulation: 8.