510(k) K960639 ยท DZE Implant, Endosseous, Root-Form
ABUTMENT SELECTION KIT
| Applicant | Nobelpharma USA, Inc., Westmont IL, US |
| Decision | Substantially Equivalent, May 14, 1996 |
| Received | Feb 14, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960639
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.