510(k) K151328 ยท DZE Implant, Endosseous, Root-Form
PURE Ceramic Implants
| Applicant | Straumann USA, Andover MA, US |
| Decision | Substantially Equivalent, Jan 11, 2016 |
| Received | May 18, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151328
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.