510(k) K080281 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PATHWAY
| Applicant | Custom Spine, Inc., Parsippany NJ, US |
| Decision | Substantially Equivalent, May 1, 2008 |
| Received | Feb 4, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080281
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.