Medical Device Manufacturer · US , Santa Rosa , CA

Medtronic Ave, Inc. - FDA 510(k) Cleared Devices

13 submissions · 2 cleared · Since 1999

13

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Medtronic Ave, Inc. Cardiovascular ✕

2 devices

1-2 of 2

Cleared Sep 27, 2000

WIRE, GUIDE, CATHETER, MODEL QSW1000

Cardiovascular · 56d

Cleared Jul 21, 2000

CATHETER, INTRAVASCULAR OCCLUDING, TEMPORARY, MODEL SOL 3510

Cardiovascular · 226d