510(k) K925776 ยท DZE Implant, Endosseous, Root-Form
BRANEMARK SYSTEM INTERLOCKING ABUTMENT/GOLD CYLIND
| Applicant | Nobelpharma USA, Inc., Chicago IL, US |
| Decision | Substantially Equivalent, Feb 10, 1994 |
| Received | Nov 16, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925776
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.