MEDTRONIC MODEL 7728 NEUROMOD

MEDTRONIC MODEL 7728 NEUROMOD is an FDA 510(k)-cleared medical device (K792311) manufactured by Medtronic Vascular. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 20, 1979. Regulation: 8.