510(k) K122322 ยท DZI Drill, Bone, Powered
PIEZOSURGERY TOUCH
| Applicant | Mectron S.P.A., Rome, IT |
| Decision | Substantially Equivalent, Dec 6, 2012 |
| Received | Aug 1, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122322
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.