510(k) K032495 ยท DZE Implant, Endosseous, Root-Form
THE LIFECORE STAGE-1 ANGLED ABUTMENT SYSTEM
| Applicant | Lifecore Biomedical, Inc., Chaska MN, US |
| Decision | Substantially Equivalent, Sep 17, 2003 |
| Received | Aug 13, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032495
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.