510(k) K221936 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Standalone ALIF Interbody Fusion System
| Applicant | Eminent Spine, Plano TX, US |
| Decision | Substantially Equivalent, Oct 17, 2022 |
| Received | Jul 1, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221936
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.