Nex-D2 CBHAD-55255
Nex-D2 CBHAD-55255 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 17 Apr 2025 (UDI-DI 00840314179791), 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 | Number00840314179791 | Date17 Apr 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK141291 | Date26 Aug 2014 | StatusActive |
Official records
- AccessGUDID record 00840314179791
- FDA 510(k) database K141291
Across registries
- FDA 510(k) K141291 decided 26 Aug 2014 Active
- FDA GUDID UDI-DI 00840314179791 listed 17 Apr 2025 Listed
Timeline
- Cleared FDA 510(k) K141291
- Listed FDA GUDID 00840314179791
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- Withdrawn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 rod
- Model / Ref / Catalog
- CBHAD-55255
- Primary DI / UDI-DI
- 00840314179791
- 510(k) Number
- FDA product code
- OSH, MNI, MNH, NKB
- GMDN term
- Bone-screw internal spinal fixation system rod
- Device class
- Class II
- Regulation number
- 888.3070
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- Size
- Outer Diameter — 5.5 MillimeterLength — 255 Millimeter
Similar devices
Other devices filed under FDA product code OSH (Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis).
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- IMPLANET SPINE SYSTEM by Implanet, S.A.
- CD HORIZON® Spinal System 1555501040 by MEDTRONIC SOFAMOR DANEK, INC.
- OP SPINE SYSTEM by ORTHOPEDIATRICS CORP.
- CREO STABILIZATION SYSTEM by GLOBUS MEDICAL, INC.
- POLARIS SPINAL SYSTEM by Biomet Spine (Aka Ebi, LLC)
- EXPEDIUM 179952060 by MEDOS INTERNATIONAL SARL
- RANGE SPINAL SYSTEM, SMALL STRATURE COMPONENTS by K2M, INC.