510(k) K994205 ยท DZE Implant, Endosseous, Root-Form
MODIFICATION OF REGULAR DIAMETER SINGLE STAGE (RDS) TPS DENTAL IMPLANT SYSTEM
| Applicant | Lifecore Biomedical, Inc., Chaska MN, US |
| Decision | Substantially Equivalent, Feb 29, 2000 |
| Received | Dec 1, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K994205
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.