← FDA Medical Device Classifications
Dural Arteriovenous Fistula Liquid Embolic
SGF · f · Unknown
Classification
- FDA Product Code
SGF- Device class
- f
- Regulation
- —
- Review panel
- NE
- Medical specialty
- Unknown
- Submission type
- 6
- GMP exempt
- N
- Life sustaining
- N
- Implant
- Y
- Third-party review
- N
Definition
Indicated for use in the treatment of intracranial dural arteriovenous fistulas.
Market data
- Cleared 510(k) submissions
- 0
- Registered establishments
- 1
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown