Medtronic Vascular

Medtronic Vascular — FDA 510(k) Submissions

Medtronic Vascular has submitted 475 FDA 510(k) premarket notifications since 1977, of which 453 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Permanent Pacemaker Electrode, Implantable Pacemaker Pulse-generator, Stimulator, Spinal-cord, Implanted (pain Relief), Catheter, Percutaneous, Electrode, Pacemaker, Temporary . Use the specialty filter in the sidebar to narrow results.