510(k) K172137 ยท DZI Drill, Bone, Powered
PIEZOTOME CUBE
| Applicant | Satelec - Acteon Group, Merignac, FR |
| Decision | Substantially Equivalent, May 3, 2018 |
| Received | Jul 17, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172137
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.