510(k) K193499 ยท DZJ Driver, Wire, And Bone Drill, Manual
DigiGuide System
| Applicant | Protomed, Inc., Westminster CO, US |
| Decision | Substantially Equivalent, Nov 4, 2020 |
| Received | Dec 17, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K193499
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.