510(k) K223251 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Hexanium PLIF
| Applicant | Spinevision, S.A.S., Antony, FR |
| Decision | Substantially Equivalent, Dec 16, 2022 |
| Received | Oct 21, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223251
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.