Medical Device Manufacturer · US , Washington , DC

Musculoskeletal Clinical Regulatory Advisers - FDA 510(k) Cleared Dev...

1 submissions · 1 cleared · Since 2010

Recent clearances: VU CPOD INTERVERTEBRAL BODU FUSION DEVICE

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Musculoskeletal Clinical Regulatory Advisers Orthopedic ✕

1 devices

1-1 of 1

Cleared Dec 16, 2010

VU CPOD INTERVERTEBRAL BODU FUSION DEVICE

Orthopedic · 216d