510(k) K200920 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Idys ALIF ZP 3DTi
| Applicant | Clariance, Sas, Beaurains, FR |
| Decision | Substantially Equivalent, May 29, 2020 |
| Received | Apr 6, 2020 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K200920
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.