510(k) K213901 · KWQ Appliance, Fixation, Spinal Intervertebral Body
Cyclops Anterior Cervical Plate System
| Applicant | Degen Medical, Florence SC, US |
| Decision | Substantially Equivalent, Jan 7, 2022 |
| Received | Dec 14, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K213901
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.