NEUROMOD COMPLEMENT #7724 DUAL CHANNEL

NEUROMOD COMPLEMENT #7724 DUAL CHANNEL is an FDA 510(k)-cleared medical device (K823742) 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 January 20, 1983. Regulation: 8.