510(k) K240803 ยท DZE Implant, Endosseous, Root-Form
Surgikor Fixation One, Abutment Blanks and Abutments
| Applicant | Surgikor, LLC, Los Angeles CA, US |
| Decision | Substantially Equivalent, Sep 12, 2024 |
| Received | Mar 25, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240803
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.