Valeo Vbr 030.7118
Valeo Vbr 030.7118 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 Feb 2020 (UDI-DI 00841732128941), 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 | Number00841732128941 | Date20 Feb 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK073505 | Date9 Jan 2008 | StatusActive |
Official records
- AccessGUDID record 00841732128941
- FDA 510(k) database K073505
Across registries
- FDA 510(k) K073505 decided 9 Jan 2008 Active
- FDA GUDID UDI-DI 00841732128941 listed 20 Feb 2020 Listed
Timeline
- Cleared FDA 510(k) K073505
- Listed FDA GUDID 00841732128941
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Valeo Vbr
- Generic name
- Spinal implant trial
- Model / reference
- 030.7118
- Primary DI / UDI-DI
- 00841732128941
- 510(k) Number
- FDA product code
- MQP
- GMDN term
- Spinal implant trial
- Device class
- Class II
- Regulation number
- 888.3060
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices in this category
Other devices filed under General internal orthopaedic fixation system implantation kit.
- NCB® 02.00024.002 by Zimmer, Inc.
- ACUMED 80-1828 by ACUMED LLC
- ACUMED 80-0731 by ACUMED LLC
- WI-407-005R: Non-Sterile, Reusable, Micro Ear Forceps 80Mm Shaft, 4.0 X 0.8Mm Serrated Jaw, Left by WELDON INSTRUMENTS
- Screwdriver 109.01.020 by Zimmer, Inc.
- 5150-9-960 by Stryker GmbH
- 0193-3800 by Stryker GmbH
- OsteoMed 320-1002 by Osteomed Corp.
- Humeca V-carrier 1.5mm, 1.5:1 6.V15-1.5/1 by Humeca B.V.