510(k) K072030 ยท DZI Drill, Bone, Powered
IMPLANT CENTER
| Applicant | Satelec - Acteon Group, Mt. Laurel NJ, US |
| Decision | Substantially Equivalent, Nov 19, 2007 |
| Received | Jul 24, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072030
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.