510(k) K013067 ยท DZE Implant, Endosseous, Root-Form
FRIALOC DENTAL IMPLANT SYSTEM
| Applicant | Friadent GmbH, Lake Forest CA, US |
| Decision | Substantially Equivalent, Apr 9, 2002 |
| Received | Sep 12, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013067
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.