510(k) K120991 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
TRANS1 INTERBODY FUSION SYSTEM
| Applicant | Trans1 Incorporated, Wilmington NC, US |
| Decision | Substantially Equivalent, Aug 23, 2012 |
| Received | Apr 2, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120991
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.