Medical Device Manufacturer · US , Minneapolis , MN

Corespine Technologies, LLC - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2009

Recent clearances: XTEND-ST NUCLEUS REMOVAL SYSTEM, MODEL 9004

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Corespine Technologies, LLC Orthopedic ✕

1 devices

1-1 of 1

Cleared Apr 30, 2009

XTEND-ST NUCLEUS REMOVAL SYSTEM, MODEL 9004

Orthopedic · 83d