Medtronic, Ireland

Medtronic, Ireland — FDA 510(k) Submissions

Medtronic, Ireland has submitted 7 FDA 510(k) premarket notifications since 2006, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter, Percutaneous, Catheters, Transluminal Coronary Angioplasty, Percutaneous, Peripheral Mechanical Thrombectomy With Aspiration . Use the specialty filter in the sidebar to narrow results.