510(k) K122519 ยท DZE Implant, Endosseous, Root-Form
DIO UF HSA INTERNAL SUB-MERGED IMPLANT SYSTEM
| Applicant | Dio Corporation, Los Angeles CA, US |
| Decision | Substantially Equivalent, May 21, 2013 |
| Received | Aug 17, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122519
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.