510(k) K150392 ยท DZJ Driver, Wire, And Bone Drill, Manual
PROPEL device
| Applicant | Propel Orthodontics, LLC, Milpitas CA, US |
| Decision | Substantially Equivalent, Sep 18, 2015 |
| Received | Feb 18, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150392
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.