510(k) K202227 · KWQ Appliance, Fixation, Spinal Intervertebral Body
Artus cervical plate system
| Applicant | Ulrich GmbH & Co. KG, Ulm, DE |
| Decision | Substantially Equivalent, Sep 14, 2020 |
| Received | Aug 7, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202227
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.