510(k) K894160 ยท DZE Implant, Endosseous, Root-Form
HAND TOOLS FOR ARTECH TYPE SS SUBMERGED SCREW IMPL
| Applicant | Artech Corp., Chantilly VA, US |
| Decision | Substantially Equivalent, Sep 28, 1989 |
| Received | Jun 14, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894160
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.