Product code SGF

Device name

Dural Arteriovenous Fistula Liquid Embolic

Medical specialty

Unknown

Device class

f

Review panel

NE

Implant

Y

Life sustaining/supporting

N

GMP exempt

N

Third party review

N

Summary malfunction reporting

Ineligible

Definition

Indicated for use in the treatment of intracranial dural arteriovenous fistulas.

Source

FDA openFDA device classification dataset