510(k) K083496 ยท DZE Implant, Endosseous, Root-Form
CAMLOG IMPLANT SYSTEM MODIFIED IMPLANTS AND ABUTMENTS
| Applicant | Altatec GmbH, San Diego CA, US |
| Decision | Substantially Equivalent, Jan 30, 2009 |
| Received | Nov 25, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083496
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.