510(k) K182195 · OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Arco-SA Lumbar Cage System
| Applicant | Neurostructures, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Nov 9, 2018 |
| Received | Aug 14, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K182195
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.