Medical Device Manufacturer · US , Austin , TX

Omni Surgical, LLC Dba Spine360 - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2014

Recent clearances: KESTREL POSTERIOR CERVICAL SPINE SYSTEM

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Omni Surgical, LLC Dba Spine360 Orthopedic ✕

1 devices

1-1 of 1

Cleared Jan 22, 2014

KESTREL POSTERIOR CERVICAL SPINE SYSTEM

Orthopedic · 196d