510(k) K180695 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
FBC 921 (ALIF)
| Applicant | Fbc Device Aps, Risskov, DK |
| Decision | Substantially Equivalent, Jul 12, 2018 |
| Received | Mar 16, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180695
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.