EZ-Track CAFB651810H
EZ-Track CAFB651810H is a Class II device made by Next Orthosurgical, cleared under FDA 510(k) K131082 on 26 Aug 2013 and listed in FDA GUDID since 3 Sep 2024 (UDI-DI 00840314131232), 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 | Number00840314131232 | Date3 Sep 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK131082 | Date26 Aug 2013 | StatusActive |
Official records
- AccessGUDID record 00840314131232
- FDA 510(k) database K131082
Across registries
- FDA 510(k) K131082 decided 26 Aug 2013 Active
- FDA GUDID UDI-DI 00840314131232 listed 3 Sep 2024 Listed
Timeline
- Cleared FDA 510(k) K131082
- Listed FDA GUDID 00840314131232
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- EZ-Track
- Generic name
- Polymeric spinal interbody fusion cage
- Model / Ref / Catalog
- CAFB651810H
- Primary DI / UDI-DI
- 00840314131232
- 510(k) Number
- FDA product code
- MAX
- GMDN term
- Polymeric spinal interbody fusion cage
- Device class
- Class II
- Regulation number
- 888.3080
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- Size
- Width — 18 MillimeterLength — 65 MillimeterHeight — 10 MillimeterAngle — 7 degree
Similar devices
Other devices filed under FDA product code MAX (Intervertebral Fusion Device With Bone Graft, Lumbar).
- CAPSTONE® Spinal System 2991422 by MEDTRONIC SOFAMOR DANEK, INC.
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- AccuLIF TL and PL Cage by Stryker Corp.
- JULIET ® Ti LL JLT-M8 50 12-S by Spineart
- Plateau Spacer System by Life Spine, Inc.
- Modulus TLIF Interbody System by Nu Vasive, Incorporated
- IB3D ALIF by Medicrea International SA
- PathLoc Lumbar Interbody Fusion Cage System by L&K Biomed
- Impulse Interbody Fusion System by Degen Medical