510(k) K080615 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ENDOSKELETON TA INTERBODY FUSION DEVICE (IBD)
| Applicant | Titan Spine, LLC, Mequon WI, US |
| Decision | Substantially Equivalent, Jun 17, 2008 |
| Received | Mar 4, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080615
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.