510(k) K203339 ยท NXC Aligner, Sequential
NEOLab Clear Aligners
| Applicant | New England Ortho Lab, Inc., Andover MA, US |
| Decision | Substantially Equivalent, Jan 6, 2021 |
| Received | Nov 12, 2020 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K203339
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.