510(k) K192029 ยท NHA Abutment, Implant, Dental, Endosseous
Straumann PUREloc abutments
| Applicant | Institut Straumann AG, Basel, CH |
| Decision | Substantially Equivalent, Oct 28, 2019 |
| Received | Jul 30, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K192029
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.