510(k) K211718 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
Venus Cervical Plate System
| Applicant | Artfx Medical, LLC, Jacksonville FL, US |
| Decision | Substantially Equivalent, Jun 28, 2022 |
| Received | Jun 4, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211718
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.