510(k) K172164 ยท DZJ Driver, Wire, And Bone Drill, Manual
PROPEL Device
| Applicant | Propel Orthodontics, LLC, Milpitas CA, US |
| Decision | Substantially Equivalent, Jan 17, 2018 |
| Received | Jul 18, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172164
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.