MINIX 8341M AND MINIX ST 8331M PULSE GENERATORS

MINIX 8341M AND MINIX ST 8331M PULSE GENERATORS is an FDA 510(k)-cleared medical device (K894055) manufactured by Medtronic Vascular. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on August 24, 1989. Regulation: 8.