510(k) K031674 ยท DZE Implant, Endosseous, Root-Form
MODIFICATION TO FRIALIT-2 DENTAL IMPLANT SYSTEM
| Applicant | Friadent GmbH, Lake Forest CA, US |
| Decision | Substantially Equivalent, Aug 14, 2003 |
| Received | May 30, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K031674
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.