510(k) K191263 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Idys ALIF TiVac
| Applicant | Clariance, Sas, Beaurains, FR |
| Decision | Substantially Equivalent, Jun 6, 2019 |
| Received | May 10, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K191263
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.