Medical Device Manufacturer · US , Westchester , IL

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

3 submissions · 3 cleared · Since 2006
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
K092825 · KWP
Orthopedic · 186d
Cleared Dec 22, 2006
APEX SPINE SYSTEM
K062513 · KWP
Orthopedic · 116d
Cleared Oct 19, 2006
OSTEOPORE TCP
K062496 · MQV
Orthopedic · 55d
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