Medical Device Manufacturer · US , South Windsor , CT

Oxford Performance Materials - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2013

Recent clearances: SpineFab Vertebral Body Replacement (VBR) System, OSTEOFAB PATIENT SPECIFIC FACIAL DEVICE, OSTEOFAB PATIENT SPECIFIC CRANIAL DEVICE

View 3 510(k) Devices ↓

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Oxford Performance Materials Neurology ✕

1 devices

1-1 of 1

Cleared Feb 07, 2013

OSTEOFAB PATIENT SPECIFIC CRANIAL DEVICE

Neurology · 232d