510(k) K220441 · KWQ Appliance, Fixation, Spinal Intervertebral Body
CYGNUS MoRe Anterior Cervical Plate System
| Applicant | MiRus, LLC, Marietta GA, US |
| Decision | Substantially Equivalent, Sep 16, 2022 |
| Received | Feb 16, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220441
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.