K261031
- 510(k) number
- K261031
- Device name
- POSEIDON ST
- Applicant
- Signus Medinzintechnik GmbH DE
- Product code
- MQP — Spinal Vertebral Body Replacement Device
- Decision date
- 2026-07-10
- Date received
- 2026-03-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K261031.pdf
Official FDA record: K261031
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.