510(k) K112787 ยท NHA Abutment, Implant, Dental, Endosseous
KERATOR
| Applicant | Kj Meditech Co., Ltd., Fullerton CA, US |
| Decision | Substantially Equivalent, Aug 8, 2012 |
| Received | Sep 26, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K112787
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.