510(k) K210320 ยท NXC Aligner, Sequential
ClearCorrect System
| Applicant | Clearcorrect, LLC, Round Rock TX, US |
| Decision | Substantially Equivalent, Aug 6, 2021 |
| Received | Feb 4, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210320
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.