510(k) K162206 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Zavation IBF
| Applicant | Zavation, LLC, Flowood MS, US |
| Decision | Substantially Equivalent, Apr 4, 2017 |
| Received | Aug 5, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162206
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.