510(k) K162390 ยท NHA Abutment, Implant, Dental, Endosseous
ET Hybrid Abutment
| Applicant | Hiossen, Inc., Fariless Hills PA, US |
| Decision | Substantially Equivalent, Jan 30, 2017 |
| Received | Aug 26, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162390
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.