
Teleflexmedical, Inc.
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Percuvance Percutaneous Surgical System is an FDA 510(k)-cleared medical device (K181852) manufactured by Teleflexmedical, 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 11, 2018. Regulation: 8.