510(k) K912262 ยท DZE Implant, Endosseous, Root-Form
HEXLOCK
| Applicant | Imtec Corp., Ardmore OK, US |
| Decision | Substantially Equivalent, Dec 10, 1991 |
| Received | May 22, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912262
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.