510(k) K083569 ยท DZI Drill, Bone, Powered
SURGYBONE
| Applicant | Silfradent S.R.L., Ormond Beach FL, US |
| Decision | Substantially Equivalent, Apr 1, 2009 |
| Received | Dec 3, 2008 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K083569
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.