510(k) K182789 ยท DZJ Driver, Wire, And Bone Drill, Manual
KLS Martin Individual Patient Solutions (IPS) Planning System
| Applicant | KLS-Martin L.P., Jacksonville FL, US |
| Decision | Substantially Equivalent, Mar 11, 2019 |
| Received | Oct 1, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182789
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.