K241762
- 510(k) number
- K241762
- Device name
- OneMark
- Applicant
- View Point Medical CA · US
- Product code
- NEU — Marker, Radiographic, Implantable
- Decision date
- 2024-09-16
- Date received
- 2024-06-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K241762.pdf
Official FDA record: K241762
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.