Medical Device Manufacturer · US , Westchester , IL

Spinecraft, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2006

Recent clearances: APEX SPINE SYSTEM 5.50 MM TITANIUM ROD & POLYAXIAL SCREW WASHER, APEX SPINE SYSTEM, OSTEOPORE TCP

View 3 510(k) Devices ↓

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Spinecraft, Inc. Orthopedic ✕

3 devices

1-3 of 3

Cleared Mar 16, 2010

APEX SPINE SYSTEM 5.50 MM TITANIUM ROD & POLYAXIAL SCREW WASHER

Orthopedic · 186d

Cleared Dec 22, 2006

APEX SPINE SYSTEM

Orthopedic · 116d

Cleared Oct 19, 2006

Orthopedic · 55d