510(k) K230993 · KWQ Appliance, Fixation, Spinal Intervertebral Body
CODA Anterior Cervical Plate System
| Applicant | Pioneer Surgical Technology, Inc D.B.A Resolve Surgical Tech, Marquette MI, US |
| Decision | Substantially Equivalent, Jun 20, 2023 |
| Received | Apr 6, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K230993
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.