510(k) K160874 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Nanovis Intervertebral Body Fusion System and FortiCore®
| Applicant | Nanovis, LLC, Columbia City IN, US |
| Decision | Substantially Equivalent, Jun 28, 2016 |
| Received | Mar 30, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K160874
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.