510(k) K191822 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Nano FortiCore, FortiCore
| Applicant | Nanovis, LLC, Columbia City IN, US |
| Decision | Substantially Equivalent, Oct 11, 2019 |
| Received | Jul 8, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191822
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.