CARDIOBLATE CRYOFLEX SURGICAL ABLATION PROBES

CARDIOBLATE CRYOFLEX SURGICAL ABLATION PROBES is an FDA 510(k)-cleared medical device (K121878) manufactured by Medtronic, Inc.. 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 November 1, 2012. Regulation: 8.