510(k) K223083 ยท DZE Implant, Endosseous, Root-Form
Straumann SLActive labeling changes
| Applicant | Institut Straumann AG, Basel, CH |
| Decision | Substantially Equivalent, Jun 22, 2023 |
| Received | Sep 30, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223083
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.