510(k) K261031 ยท MQP Spinal Vertebral Body Replacement Device
POSEIDON ST
| Applicant | Signus Medinzintechnik GmbH, Alzenau, DE |
| Decision | Substantially Equivalent, Jul 10, 2026 |
| Received | Mar 30, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K261031
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.