510(k) K183138 ยท NHA Abutment, Implant, Dental, Endosseous
Certain BellaTek Express and BellaTek Flex Abutments
| Applicant | Biomet 3i, Palm Beach Gardens FL, US |
| Decision | Substantially Equivalent, Jul 2, 2019 |
| Received | Nov 13, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183138
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.