510(k) K160436 ยท NHA Abutment, Implant, Dental, Endosseous
CreoDent Solidex Custom Abutment
| Applicant | Creodent Prosthetics, Ltd., New York NY, US |
| Decision | Substantially Equivalent, Sep 29, 2016 |
| Received | Feb 17, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160436
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.