510(k) K911735 ยท DZE Implant, Endosseous, Root-Form
ARTECH ARDENT IV - TYPE CLYLINDER IMPLANT
| Applicant | Artech Corp., Chantilly VA, US |
| Decision | Substantially Equivalent, Mar 5, 1992 |
| Received | Apr 17, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911735
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.