510(k) K000889 ยท DZE Implant, Endosseous, Root-Form
SENOJ IMPLANT SYSTEM
| Applicant | Senoj Biocare, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Apr 27, 2001 |
| Received | Mar 20, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000889
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.