510(k) K083550 ยท DZE Implant, Endosseous, Root-Form
STRAUMANN DENTAL IMPLANT SYSTEM
| Applicant | Straumann USA, Andover MA, US |
| Decision | Substantially Equivalent, Feb 26, 2009 |
| Received | Dec 1, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083550
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.