510(k) K090566 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PATHWAY AVID
| Applicant | Custom Spine, Inc., Parsippany NJ, US |
| Decision | Substantially Equivalent, Jun 1, 2009 |
| Received | Mar 3, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090566
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.