510(k) K220115 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
ANTARES 3DR Standalone Anterior Lumbar Interbody Fusion System
| Applicant | MiRus, LLC, Marietta GA, US |
| Decision | Substantially Equivalent, May 13, 2022 |
| Received | Jan 14, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220115
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.