510(k) K250446 · KWQ Appliance, Fixation, Spinal Intervertebral Body
Frida Anterior Cervical Plate System
| Applicant | Spineup, Inc., Hollywood FL, US |
| Decision | Substantially Equivalent, May 23, 2025 |
| Received | Feb 14, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250446
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.