510(k) K060274 ยท DZI Drill, Bone, Powered
PIEZOTOME
| Applicant | Satelec, Mt. Laurel NJ, US |
| Decision | Substantially Equivalent, May 1, 2006 |
| Received | Feb 2, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060274
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.