510(k) K192993 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
SCARLET AL-T
| Applicant | Spineart, Geneva, CH |
| Decision | Substantially Equivalent, Jan 22, 2020 |
| Received | Oct 25, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K192993
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.