510(k) K180477 ยท DZE Implant, Endosseous, Root-Form
Straumann PURE Ceramic Implant System
| Applicant | Institut Straumann AG, Basel, CH |
| Decision | Substantially Equivalent, Jan 4, 2019 |
| Received | Feb 22, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180477
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.