510(k) K172465 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Idys TLIF 3DTi Cages
| Applicant | Clariance, Sas, Beaurains, FR |
| Decision | Substantially Equivalent, Dec 15, 2017 |
| Received | Aug 14, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172465
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.