510(k) K143143 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PATHWAY ELIF
| Applicant | Custom Spine, Inc., Parsippany NJ, US |
| Decision | Substantially Equivalent, Jul 22, 2015 |
| Received | Nov 3, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143143
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.