510(k) K924121 ยท DZE Implant, Endosseous, Root-Form
STERI-OSS SCREW STYLE ITIANIUM IMPLANT
| Applicant | Steri-Oss, Inc., Anaheim CA, US |
| Decision | Substantially Equivalent, Dec 10, 1993 |
| Received | Aug 14, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924121
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.