510(k) K895267 ยท DZE Implant, Endosseous, Root-Form
ARTECH TYPE SS-HA SUBMERGED SCREW IMPLANT
| Applicant | Artech Corp., Chantilly VA, US |
| Decision | Substantially Equivalent, Apr 10, 1990 |
| Received | Aug 23, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895267
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.