510(k) K193000 · OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
Hexanium® ACIF
| Applicant | Spinevision, S.A.S., Antony, FR |
| Decision | Substantially Equivalent, Oct 20, 2020 |
| Received | Oct 28, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K193000
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.