SGF — Dural Arteriovenous Fistula Liquid Embolic Class f
FDA product code SGF covers "Dural Arteriovenous Fistula Liquid Embolic", a Class f medical device. Submissions are reviewed by the Unknown panel. Devices under this code are implants.
Classification Details
- Product Code
- SGF
- Device Class
- Class f
- Regulation Number
- Submission Type
- Review Panel
- NE
- Medical Specialty
- Unknown
- Implant
- Yes
Definition
Indicated for use in the treatment of intracranial dural arteriovenous fistulas.