510(k) K102957 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
CUTTING EDGE SPINE INTERBODY FUSION DEVICE
| Applicant | Cutting Edge Spine, LLC, Waxhaw NC, US |
| Decision | Substantially Equivalent, Apr 28, 2011 |
| Received | Oct 5, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102957
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.