510(k) K913228 ยท DZE Implant, Endosseous, Root-Form
INTERPORE IMZ CYLINDER IMPLANT SYSTEM
| Applicant | Interpore Intl., Irvine CA, US |
| Decision | Substantially Equivalent, Oct 13, 1992 |
| Received | Jul 22, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913228
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.