510(k) K151276 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
DePuy Synthes T-PAL Ti Spacer
| Applicant | Synthes USA Products, LLC, Raynham MA, US |
| Decision | Substantially Equivalent, Jun 18, 2015 |
| Received | May 13, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K151276
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.