510(k) K911593 ยท DZE Implant, Endosseous, Root-Form
STERI-OSS DUAL COATED CYLINDRICAL IMPLANTS
| Applicant | Steri-Oss, Inc., Anaheim CA, US |
| Decision | Substantially Equivalent, Oct 7, 1993 |
| Received | Apr 9, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911593
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.