SGF

Dural Arteriovenous Fistula Liquid Embolic

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.

Definition text from the FDA device classification database (U.S. federal government work, public domain).

Official FDA classification page: SGF
Classification and pathway per current FDA publications. Data from openFDA (CC0).