Nex-D2 CBFDJ-60095
Nex-D2 CBFDJ-60095 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 6 Sep 2024 (UDI-DI 00840314168269), 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 | Number00840314168269 | Date6 Sep 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK141291 | Date26 Aug 2014 | StatusActive |
Official records
- AccessGUDID record 00840314168269
- FDA 510(k) database K141291
Across registries
- FDA 510(k) K141291 decided 26 Aug 2014 Active
- FDA GUDID UDI-DI 00840314168269 listed 6 Sep 2024 Listed
Timeline
- Cleared FDA 510(k) K141291
- Listed FDA GUDID 00840314168269
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- Withdrawn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 / Ref / Catalog
- CBFDJ-60095
- Primary DI / UDI-DI
- 00840314168269
- 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
- Size
- Outer Diameter — 6 MillimeterLength — 95 Millimeter
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Other devices filed under FDA product code NKB (Thoracolumbosacral Pedicle Screw System).
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- Erisma®-LP 13028575 by Clariance, Inc.
- TRIO TRAUMA SPINAL SYSTEM by Stryker Corp.
- CD HORIZON® Spinal System 54840005545 by MEDTRONIC SOFAMOR DANEK, INC.