AEx Generator; PlasmaBlade T

AEx Generator; PlasmaBlade T is an FDA 510(k)-cleared medical device (K143175) manufactured by Medtronic Advanced Energy. 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 December 30, 2014. Regulation: 8.