510(k) K132738 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
COGENT MED-LIF
| Applicant | Cogent Spine, LLC, Solana Beach CA, US |
| Decision | Substantially Equivalent, Apr 15, 2014 |
| Received | Sep 3, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132738
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.