510(k) K082532 ยท DZI Drill, Bone, Powered
STRAUMANN GUIDED INSTRUMENTS
| Applicant | Straumann USA, Andover MA, US |
| Decision | Substantially Equivalent, Oct 21, 2008 |
| Received | Sep 2, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082532
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.