ITC BUNJI COIL (MODIFICATION)

ITC BUNJI COIL (MODIFICATION) is an FDA 510(k)-cleared medical device (K920324) manufactured by Interventional Therapeutics Corp.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 28, 1992. Regulation: 8.