510(k) K083561 ยท DZE Implant, Endosseous, Root-Form
NEOSS PROACTIVE IMPLANT
| Applicant | Neoss, Ltd., Alexandria VA, US |
| Decision | Substantially Equivalent, Feb 11, 2009 |
| Received | Dec 2, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K083561
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.