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Neuwave Medical, Inc.
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CERTUS 140 MICROWAVE ABLATION SYSTEM AND ACCESSORIES, MODEL CERTUS 140 is an FDA 510(k)-cleared medical device (K100744) manufactured by Neuwave Medical, 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 October 21, 2010. Regulation: 8.