510(k) K180437 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Hexanium® TLIF
| Applicant | Spinevision, S.A.S., Antony, FR |
| Decision | Substantially Equivalent, May 4, 2018 |
| Received | Feb 20, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180437
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.