510(k) K210855 ยท DZE Implant, Endosseous, Root-Form
Straumann BLX Implant System
| Applicant | Institut Straumann AG, Basel, CH |
| Decision | Substantially Equivalent, Jun 21, 2021 |
| Received | Mar 23, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210855
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.