510(k) K920909 ยท DZE Implant, Endosseous, Root-Form
HEXLOCK SCREW
| Applicant | Imtec Corp., Ardmore OK, US |
| Decision | Substantially Equivalent, Jan 12, 1993 |
| Received | Feb 27, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920909
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.