510(k) K203737 ยท NXC Aligner, Sequential
Spark Clear Aligner System
| Applicant | Ormco Corporation, Brea CA, US |
| Decision | Substantially Equivalent, Mar 22, 2021 |
| Received | Dec 22, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203737
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.