SGF
- Product code
- SGF
- Device name
- Dural Arteriovenous Fistula Liquid Embolic
- Device class
- Class F
- Medical specialty
- Unknown
- Marketing pathway
- HDE - Humanitarian Device Exemption
- Flag
- Implant
FDA classification definition
Indicated for use in the treatment of intracranial dural arteriovenous fistulas.
Official FDA classification page: SGF
Classification and pathway per current FDA publications. Data from openFDA (CC0).