510(k) K911112 ยท DZE Implant, Endosseous, Root-Form
DEVICE PART NUMBERS: - 1400 SERIES
| Applicant | Minimatic Implant Technology, Deerfield Beach FL, US |
| Decision | Substantially Equivalent, Jun 10, 1991 |
| Received | Feb 13, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911112
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.