510(k) K970776 ยท DZE Implant, Endosseous, Root-Form
LIFECORE O-RING ABUTMENT;LIFECORE DALLA BONA ABUTMENT
| Applicant | Lifecore Biomedical, Inc., Chaska MN, US |
| Decision | Substantially Equivalent, May 27, 1997 |
| Received | Mar 4, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970776
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.