510(k) K955492 ยท DZE Implant, Endosseous, Root-Form
INTERPORE IMZ CYL IMPLANT & CYL HEX IMPLT
| Applicant | Interpore Intl., Irvine CA, US |
| Decision | Substantially Equivalent, Jan 30, 1996 |
| Received | Dec 1, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955492
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.