510(k) K173082 · OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Arco-SA Lumbar Cage System
| Applicant | Neurostructures, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Mar 29, 2018 |
| Received | Sep 29, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173082
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.