
Percudisc, Inc.
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PERCUDISC PLDD DELIVERY SYSTEM/PROCEDURE KIT is an FDA 510(k)-cleared medical device (K920673) manufactured by Percudisc, 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 August 12, 1992. Regulation: 8.