510(k) K190662 ยท DZE Implant, Endosseous, Root-Form
MRI Compatibility for Existing Straumann Dental Implant Systems
| Applicant | Straumann USA, LLC, Andover MA, US |
| Decision | Substantially Equivalent, Jun 17, 2019 |
| Received | Mar 15, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190662
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.