510(k) K931468 ยท DZE Implant, Endosseous, Root-Form
RESTORE HEX CYLINDER ENDOSSEOUS SYSTEM
| Applicant | Lifecore Biomedical, Inc., Chaska MN, US |
| Decision | Substantially Equivalent, Jul 12, 1994 |
| Received | Mar 24, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931468
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.