510(k) K150296 ยท NHA Abutment, Implant, Dental, Endosseous
Biodenta Customized Abutment-Hybrid
| Applicant | Biodenta Swiss AG, Berneck, CH |
| Decision | Substantially Equivalent, Jul 2, 2015 |
| Received | Feb 6, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150296
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.