510(k) K053629 ยท DZE Implant, Endosseous, Root-Form
ANCHOR PLUS/NEO ANCHOR PLUS
| Applicant | Kj Meditech, Flintville TN, US |
| Decision | Substantially Equivalent, May 31, 2006 |
| Received | Dec 29, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K053629
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.