510(k) K183259 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Idys TLIF TiVac
| Applicant | Clariance, Sas, Beaurains, FR |
| Decision | Substantially Equivalent, Mar 1, 2019 |
| Received | Nov 21, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183259
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.