Medical Device Manufacturer · FR , Chassieu

Renishaw Mayfield Sarl - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2014

Recent clearances: neuromate Gen III, neuromate Gen III, NEUROMATE FRAMELESS GEN II

View 3 510(k) Devices ↓

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Renishaw Mayfield Sarl Neurology ✕

3 devices

1-3 of 3

Cleared Jul 26, 2018

neuromate Gen III

Neurology · 28d

Cleared Apr 24, 2018

neuromate Gen III

Neurology · 90d

Cleared Apr 29, 2014

NEUROMATE FRAMELESS GEN II

Neurology · 238d