510(k) K162358 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
T-PAL Spacer System, T-PAL Titanium Spacer System, SYNFIX Evolution System
| Applicant | Synthes USA Products, LLC, Raynham MA, US |
| Decision | Substantially Equivalent, Nov 1, 2016 |
| Received | Aug 23, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162358
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.