510(k) K202190 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Oculus-SA Lumbar Cage System
| Applicant | Neurostructures, Irvine CA, US |
| Decision | Substantially Equivalent, Oct 2, 2020 |
| Received | Aug 5, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202190
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.