510(k) K171769 ยท DZE Implant, Endosseous, Root-Form
Straumann PURE Ceramic Implants
| Applicant | Straumann USA, LLC (On Behalf of Institut Straumann Ag), Andover MA, US |
| Decision | Substantially Equivalent, Nov 14, 2017 |
| Received | Jun 14, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171769
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.