510(k) K091331 ยท DZI Drill, Bone, Powered
PIEZOTOME 2
| Applicant | Satelec, Mt. Laurel NJ, US |
| Decision | Substantially Equivalent, Dec 11, 2009 |
| Received | May 5, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091331
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.