510(k) K160475 ยท DZE Implant, Endosseous, Root-Form
Ritter Dental Implant System
| Applicant | Ritter Implants GmbH & Co. KG, Biberach, DE |
| Decision | Substantially Equivalent, Dec 14, 2016 |
| Received | Feb 19, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160475
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.