510(k) K230836 ยท NEU Marker, Radiographic, Implantable
SchurSign Tissue Marker
| Applicant | Surgmark GmbH, Hamburg, DE |
| Decision | Substantially Equivalent, Jan 23, 2024 |
| Received | Mar 27, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230836
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.