510(k) K043195 ยท DZE Implant, Endosseous, Root-Form
NEO IMPLANT SYSTEM
| Applicant | Neoss, Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Mar 7, 2005 |
| Received | Nov 18, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K043195
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.