510(k) K181739 ยท NXC Aligner, Sequential
Invisalign System with Mandibular Advancement Feature
| Applicant | Align Technology, Inc., San Jose CA, US |
| Decision | Substantially Equivalent, Oct 26, 2018 |
| Received | Jul 2, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181739
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.