510(k) K171326 ยท DZI Drill, Bone, Powered
Piezosurgery White
| Applicant | Mectron S.P.A., Carasco, IT |
| Decision | Substantially Equivalent, Apr 13, 2018 |
| Received | May 5, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171326
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.