510(k) K210359 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Hexanium TLIF
| Applicant | Spinevision, S.A.S., Batiment E, FR |
| Decision | Substantially Equivalent, Mar 10, 2021 |
| Received | Feb 8, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K210359
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.