510(k) K151248 ยท DZI Drill, Bone, Powered
PIEZOSURGERY WHITE
| Applicant | Mectron S.P.A., Carasco, IT |
| Decision | Substantially Equivalent, Sep 4, 2015 |
| Received | May 11, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151248
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.