510(k) K123784 ยท DZE Implant, Endosseous, Root-Form
STRAUMANN DENTAL IMPLANT SYSTEM
| Applicant | Straumann USA, LLC, Andover MA, US |
| Decision | Substantially Equivalent, Apr 10, 2013 |
| Received | Dec 10, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123784
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.