510(k) K990983 ยท DZE Implant, Endosseous, Root-Form
MODIFICATION TO IMTEC SENDAX MDI
| Applicant | Imtec Corp., Ardmore OK, US |
| Decision | Substantially Equivalent, Apr 13, 1999 |
| Received | Mar 24, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K990983
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.