510(k) K161485 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Nanovis Intervertebral Body Fusion System and Forticore(R)
| Applicant | Nanovis, LLC, Columbia City IN, US |
| Decision | Substantially Equivalent, Sep 6, 2016 |
| Received | May 31, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161485
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.