510(k) K190666 · KWQ Appliance, Fixation, Spinal Intervertebral Body
CYGNUS Anterior Cervical Plate System
| Applicant | MiRus, LLC, Marietta GA, US |
| Decision | Substantially Equivalent, May 9, 2019 |
| Received | Mar 15, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190666
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.