510(k) K171312 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
FortiCore®
| Applicant | Nanovis, LLC, Columbia City IN, US |
| Decision | Substantially Equivalent, Jan 22, 2018 |
| Received | May 4, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171312
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.