V-Trak 8510-0408-A2
V-Trak 8510-0408-A2 is a Class II device made by Microvention Inc., listed in FDA GUDID since 30 Apr 2025 (UDI-DI 00816777020949), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00816777020949 | Date30 Apr 2025 | StatusListed |
Official records
- AccessGUDID record 00816777020949
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- V-Trak
- Generic name
- Neurovascular embolization coil
- Model / Ref / Catalog
- 8510-0408-A2, 8510-0408
- Primary DI / UDI-DI
- 00816777020949
- FDA product code
- KRD, HCG
- GMDN term
- Neurovascular embolization coil
- Device class
- Class II
- Regulation number
- 870.3300, 882.5950
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
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