510(k) K240501 · NXC Aligner, Sequential
Spark Clear Aligner System
| Applicant | Ormco Corporation, Brea CA, US |
| Decision | Substantially Equivalent, Oct 11, 2024 |
| Received | Feb 21, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240501
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.