Valeo Vbr 11.009.1622
Valeo Vbr 11.009.1622 is a Class II device made by CTL Medical Corporation, cleared under FDA 510(k) K073505 on 9 Jan 2008 and listed in FDA GUDID since 20 Sep 2023 (UDI-DI 00841732155053), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00841732155053 | Date20 Sep 2023 | StatusListed |
| United States | FDA 510(k)SESE | NumberK073505 | Date9 Jan 2008 | StatusActive |
Official records
- AccessGUDID record 00841732155053
- FDA 510(k) database K073505
Across registries
- FDA 510(k) K073505 decided 9 Jan 2008 Active
- FDA GUDID UDI-DI 00841732155053 listed 20 Sep 2023 Listed
Timeline
- Cleared FDA 510(k) K073505
- Listed FDA GUDID 00841732155053
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Valeo Vbr
- Generic name
- Ceramic spinal interbody fusion cage
- Model / reference
- 11.009.1622
- Primary DI / UDI-DI
- 00841732155053
- 510(k) Number
- FDA product code
- MQP
- GMDN term
- Ceramic spinal interbody fusion cage
- Device class
- Class II
- Regulation number
- 888.3060
- GUDID distribution status
- In Commercial Distribution
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