510(k) K103577 ยท DZE Implant, Endosseous, Root-Form
TRINON Q & Q3 IMPLANT SYSTEM
| Applicant | Trinon Titanium GmbH, Tuttlingen, DE |
| Decision | Substantially Equivalent, Jul 3, 2012 |
| Received | Dec 6, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103577
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.