510(k) K090452 ยท DZE Implant, Endosseous, Root-Form
NEOSS IMPLANT SYSTEM 03.25
| Applicant | Neoss, Ltd., Alexandria VA, US |
| Decision | Substantially Equivalent, May 22, 2009 |
| Received | Feb 23, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090452
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.