510(k) K173961 ยท DZE Implant, Endosseous, Root-Form
Straumann BLX Implant System
| Applicant | Institut Straumann AG, Basel, CH |
| Decision | Substantially Equivalent, Jun 5, 2018 |
| Received | Dec 28, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173961
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.