SGU — Neurovascular Liquid Embolic Agent Class III

FDA Device Classification

FDA product code SGU covers "Neurovascular Liquid Embolic Agent", a Class III medical device. Submissions are reviewed by the Unknown panel. Devices under this code are implants.

Classification Details

Product Code
SGU
Device Class
Class III
Regulation Number
Submission Type
Review Panel
NE
Medical Specialty
Unknown
Implant
Yes

Definition

Arterial occlusion of the middle meningeal artery for treatment of symptomatic subdural hematoma.