510(k) K080588 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SCIENT'X TRIBECA VBR
| Applicant | Scient'X USA, Inc., Maitland FL, US |
| Decision | Substantially Equivalent, May 30, 2008 |
| Received | Mar 3, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080588
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.