510(k) K160581 ยท DZE Implant, Endosseous, Root-Form
K3PRO Konus Additional Abutments and Implants
| Applicant | Argon Med. Productions Vertriebs Gesellschaft Mbh CO KG, Bingen Am Rhein, DE |
| Decision | Substantially Equivalent, Mar 24, 2017 |
| Received | Mar 1, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160581
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.