NEUROMOD STIMULATOR MODEL 3723

NEUROMOD STIMULATOR MODEL 3723 is an FDA 510(k)-cleared medical device (K780186) 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 March 1, 1978. Regulation: 8.