510(k) K922732 ยท DZE Implant, Endosseous, Root-Form
INTERPORE CYLINDRICAL HEX IMPLANT, 3.3 MM DIAMETER
| Applicant | Interpore Intl., Irvine CA, US |
| Decision | Substantially Equivalent, Feb 10, 1994 |
| Received | Jun 8, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922732
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.