Nex-D2 CBAAJ-40060
Nex-D2 CBAAJ-40060 is a Class II device made by Next Orthosurgical, cleared under FDA 510(k) K141291 on 26 Aug 2014 and listed in FDA GUDID since 20 Aug 2024 (UDI-DI 00840314111852), 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 | Number00840314111852 | Date20 Aug 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK141291 | Date26 Aug 2014 | StatusActive |
Official records
- AccessGUDID record 00840314111852
- FDA 510(k) database K141291
Across registries
- FDA 510(k) K141291 decided 26 Aug 2014 Active
- FDA GUDID UDI-DI 00840314111852 listed 20 Aug 2024 Listed
Timeline
- Cleared FDA 510(k) K141291
- Listed FDA GUDID 00840314111852
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Nex-D2
- Generic name
- Bone-screw internal spinal fixation system, non-sterile
- Model / reference
- CBAAJ-40060
- Primary DI / UDI-DI
- 00840314111852
- 510(k) Number
- FDA product code
- NKB, OSH, MNI, MNH
- GMDN term
- Bone-screw internal spinal fixation system, non-sterile
- Device class
- Class II
- Regulation number
- 888.3070
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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