Medtronic Ave, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CATHETER, INTRAVASCULAR OCCLUDING, TEMPORARY, MODEL SOL 3510, MEDTRONIC AVE BRIDGE STENT, MEDTRONIC AVE BRIDGE STENT
13
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Medtronic Ave, Inc. Cardiovascular ✕
2 devices