510(k) K061323 ยท DZE Implant, Endosseous, Root-Form
MODIFICATION TO RELIADENT DENTAL IMPLANT SYSTEM
| Applicant | Bioinfera, Inc., Beachwood OH, US |
| Decision | Substantially Equivalent, May 23, 2007 |
| Received | May 11, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061323
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.