510(k) K080314 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SPINAL USA INTERBODY FUSION DEVICE
| Applicant | Spinal USA, Flowood MS, US |
| Decision | Substantially Equivalent, May 13, 2008 |
| Received | Feb 6, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080314
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.