FDA product code SGF: Dural Arteriovenous Fistula Liquid Embolic
SGF is the FDA product code for dural arteriovenous fistula liquid embolic. It is a HDE device, reviewed by the Neurology panel. Devices under SGF reach the market by Unclassified; FDA lists no cleared 510(k)s for it.
Definition
Indicated for use in the treatment of intracranial dural arteriovenous fistulas.
Classification
| Field | Value |
|---|---|
| Device name | Dural Arteriovenous Fistula Liquid Embolic |
| Device class | HDE |
| Review panel | NE — Neurology |
| Medical specialty | Unknown |
| Premarket route | Unclassified |
| Implant | Yes |
Recalls for SGF devices
openFDA lists no recalls for product code SGF.
Frequently asked questions
What is FDA product code SGF?
SGF is the FDA product code for dural arteriovenous fistula liquid embolic. It is a HDE device, reviewed by the Neurology panel.
What device class is SGF?
HDE. Typical premarket route: Unclassified.
Next steps
- Run an FDA pathway report with predicate devices for product code SGF
- Run a recall and safety report across every SGF manufacturer
- Watch product code SGF for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.