510(k) K003226 ยท DZE Implant, Endosseous, Root-Form
THE LIFECORE STAGE-1 SINGLE STAGE RBM DENTAL IMPLANT SYSTEM
| Applicant | Lifecore Biomedical, Inc., Chaska MN, US |
| Decision | Substantially Equivalent, Jan 12, 2001 |
| Received | Oct 16, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K003226
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.