Medical Device Manufacturer · US , Minneapolis, , MN

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

1 submissions · 1 cleared · Since 2005

Recent clearances: MODEL 3873 1* 8 AND MODEL 3874 1* 8 COMPACT TEST STIMULATION LEADS

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Medtronic Inc.,Neurological Division. Neurology ✕

1 devices

1-1 of 1

Cleared Jul 28, 2005

MODEL 3873 1* 8 AND MODEL 3874 1* 8 COMPACT TEST STIMULATION LEADS

Neurology · 27d