510(k) K231766 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
Skyway Anterior Cervical Plate System
| Applicant | Kyocera Medical Technologies Inc. (KMTI), Redlands CA, US |
| Decision | Substantially Equivalent, Sep 12, 2023 |
| Received | Jun 16, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231766
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.