510(k) K233215 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
icotec Anterior Cervical Plate System
| Applicant | Icotec AG, 9450 Altstaetten (Sg), CH |
| Decision | Substantially Equivalent, May 17, 2024 |
| Received | Sep 26, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233215
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.