Medtronic Cardiac Surgery

Medtronic Cardiac Surgery — FDA 510(k) Submissions

Medtronic Cardiac Surgery has submitted 1 FDA 510(k) premarket notifications since 2024, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Reservoir, Blood, Cardiopulmonary Bypass . Use the specialty filter in the sidebar to narrow results.