510(k) K993894 ยท DZE Implant, Endosseous, Root-Form
LIFECORE SINGLE TOOTH ABUTMENT SYSTEM
| Applicant | Lifecore Biomedical, Inc., Chaska MN, US |
| Decision | Substantially Equivalent, Mar 8, 2000 |
| Received | Nov 16, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993894
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.