510(k) K243670 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Idys® LIF
| Applicant | Clariance, Beaurains, FR |
| Decision | Substantially Equivalent, Dec 31, 2024 |
| Received | Nov 27, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K243670
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.