510(k) K033767 ยท DZE Implant, Endosseous, Root-Form
DUAL TOP ANCHOR SYSTEM SCREWS
| Applicant | Jeil Medical Corporation, Deer Field IL, US |
| Decision | Substantially Equivalent, Feb 24, 2004 |
| Received | Dec 3, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033767
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.