510(k) K964739 ยท DZE Implant, Endosseous, Root-Form
STERI-OSS TIODIZED SCREW
| Applicant | Steri-Oss, Inc., Yorba Linda CA, US |
| Decision | Substantially Equivalent, Mar 31, 1997 |
| Received | Nov 26, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964739
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.