510(k) K220182 · KWQ Appliance, Fixation, Spinal Intervertebral Body
Aggeris-C
| Applicant | Clariance, Beaurains, FR |
| Decision | Substantially Equivalent, Mar 30, 2022 |
| Received | Jan 21, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220182
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.