510(k) K180076 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Ti 3Z Interbody System
| Applicant | Zavation Medical Products, LLC, Flowood MS, US |
| Decision | Substantially Equivalent, Jul 27, 2018 |
| Received | Jan 10, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180076
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.