K232865
- 510(k) number
- K232865
- Device name
- Magseed Pro Magnetic Marker System
- Applicant
- Endomagnetics Ltd., GB
- Product code
- NEU — Marker, Radiographic, Implantable
- Decision date
- 2024-06-28
- Date received
- 2023-09-15
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K232865.pdf
Official FDA record: K232865
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.