IMPLANTECH JEJ PERI-PYRIFORM IMPLANT

IMPLANTECH JEJ PERI-PYRIFORM IMPLANT is an FDA 510(k)-cleared medical device (K962824) manufactured by Implantech Associates, 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 2, 1996. Regulation: 8.