510(k) K150814 ยท NHA Abutment, Implant, Dental, Endosseous
Straumann Screw-Retained Abutment
| Applicant | Straumann USA, LLC, Andover MA, US |
| Decision | Substantially Equivalent, Aug 10, 2015 |
| Received | Mar 27, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150814
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.