510(k) K172430 ยท NHA Abutment, Implant, Dental, Endosseous
ArgenIS Titanium Abutments
| Applicant | Argen Corporation, San Diego CA, US |
| Decision | Substantially Equivalent, May 18, 2018 |
| Received | Aug 11, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172430
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.