510(k) K242516 · NKG Posterior Cervical Screw System
EUROPA Posterior Cervical Fusion System
| Applicant | MiRus, LLC, Marietta GA, US |
| Decision | Substantially Equivalent, Nov 19, 2024 |
| Received | Aug 23, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242516
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.