510(k) K232154 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
MiRus 3DR Lateral Lumbar Interbody Fusion System with Integrated Plate Fixation
| Applicant | MiRus, LLC, Marietta GA, US |
| Decision | Substantially Equivalent, Sep 11, 2023 |
| Received | Jul 20, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232154
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.