Medical Device Manufacturer · US , Cambridge , MA

Etex Corp. - FDA 510(k) Cleared Devices

18 submissions · 17 cleared · Since 1994

18

Total

17

Cleared

0

Denied

FDA 510(k) Regulatory Record - Etex Corp. Neurology ✕

2 devices

1-2 of 2

Cleared Oct 24, 2003

CAP BONE SUBSTITUTE MATERIAL

Neurology · 91d

Cleared Nov 25, 1998

BSM- BONE SUBSTITUTE MATERIAL

Neurology · 89d