510(k) K222493 · KWQ Appliance, Fixation, Spinal Intervertebral Body
CODA Anterior Cervical Plate System
| Applicant | Pioneer Surgical Technology, Inc., Marquette MI, US |
| Decision | Substantially Equivalent, Nov 18, 2022 |
| Received | Aug 18, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222493
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.