510(k) K200919 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Idys ALIF 3DTi
| Applicant | Clariance, Beaurains, FR |
| Decision | Substantially Equivalent, Apr 12, 2021 |
| Received | Apr 6, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200919
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.