Medical Device Manufacturer · US , Westmont , IL

SpineCraft

2 submissions · 2 cleared · Since 2009
2
Total
2
Cleared
0
Denied

SpineCraft — FDA 510(k) Submissions

SpineCraft has submitted 2 FDA 510(k) premarket notifications since 2009, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Intervertebral Fusion Device With Bone Graft, Cervical, Appliance, Fixation, Spinal Intervertebral Body . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
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