510(k) K131557 ยท DZE Implant, Endosseous, Root-Form
RITTER IMPLANT SYSTEM
| Applicant | Ritter Implants GmbH CO KG, Monroe CT, US |
| Decision | Substantially Equivalent, May 9, 2014 |
| Received | May 29, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131557
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.