MODEL 3587A RESUME EPIDURAL LEAD

MODEL 3587A RESUME EPIDURAL LEAD is an FDA 510(k)-cleared medical device (K884948) 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 16, 1989. Regulation: 8.