510(k) K041651 ยท DZE Implant, Endosseous, Root-Form
STRYKER LEIBINGER SKELETAL ANCHORING SYSTEM
| Applicant | Stryker Leibinger, Kalamazoo MI, US |
| Decision | Substantially Equivalent, Sep 30, 2004 |
| Received | Jun 17, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041651
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.