EZ-Track CJBB151310G
EZ-Track CJBB151310G is a Class II device made by Next Orthosurgical, cleared under FDA 510(k) K161608 on 30 Sep 2016 and listed in FDA GUDID since 12 Sep 2024 (UDI-DI 00840314137753), 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 | Number00840314137753 | Date12 Sep 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK161608 | Date30 Sep 2016 | StatusActive |
Official records
- AccessGUDID record 00840314137753
- FDA 510(k) database K161608
Across registries
- FDA 510(k) K161608 decided 30 Sep 2016 Active
- FDA GUDID UDI-DI 00840314137753 listed 12 Sep 2024 Listed
Timeline
- Cleared FDA 510(k) K161608
- Listed FDA GUDID 00840314137753
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- Withdrawn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
- CJBB151310G
- Primary DI / UDI-DI
- 00840314137753
- 510(k) Number
- FDA product code
- ODP
- 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 — 15 MillimeterLength — 13 MillimeterHeight — 10 MillimeterAngle — 6 degree
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