510(k) K100210 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
TRANS1 LATERAL INTERVERTEBRAL FUSION DEVICE, T
| Applicant | Trans1 Incorporated, Wilmington NC, US |
| Decision | Substantially Equivalent, Aug 26, 2010 |
| Received | Jan 25, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100210
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.