
Medtronic, Inc.
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PROSTIVA RF THERAPY HAND PIECE PROSTIVA RF THERAPY RF GENERATOR is an FDA 510(k)-cleared medical device (K113380) 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 14, 2012. Regulation: 8.