510(k) K141159 ยท DZE Implant, Endosseous, Root-Form
KONUS DENTAL IMPLANT SYSTEM
| Applicant | Argon Med. Productions Vertriebs Gesellschaft Mbh, Marshfield WI, US |
| Decision | Substantially Equivalent, Mar 11, 2015 |
| Received | May 5, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141159
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.