510(k) K241722 · NHA Abutment, Implant, Dental, Endosseous
Elos Accurate® Hybrid Base; Elos Accurate® Customized Abutment
| Applicant | Elos Medtech Pinol A/S, Goerloese, DK |
| Decision | Substantially Equivalent, Sep 13, 2024 |
| Received | Jun 14, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241722
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.