510(k) K252327 · NKG Posterior Cervical Screw System
CMORE® CT System; CMORE® CT System Navigated Instruments
| Applicant | Icotec AG, Altstaetten, CH |
| Decision | Substantially Equivalent, Nov 12, 2025 |
| Received | Jul 25, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K252327
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.