510(k) K944158 ยท DZE Implant, Endosseous, Root-Form
STERI-OSS TITANIUM ALLOY SCREW SERIES IMPLANT FOR SINGLE STAGE SURGICAL PLACEMENT
| Applicant | Steri-Oss, Inc., Yorba Linda CA, US |
| Decision | Substantially Equivalent, Mar 29, 1995 |
| Received | Aug 26, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K944158
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.