MEDTRONIC MODEL 3998 LEAD

MEDTRONIC MODEL 3998 LEAD is an FDA 510(k)-cleared medical device (K971756) 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 February 2, 1998. Regulation: 8.