510(k) K181818 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Scarlet AL-T
| Applicant | Spineart, Plan Les Ouates, CH |
| Decision | Substantially Equivalent, Oct 9, 2018 |
| Received | Jul 9, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181818
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.