Creo 1067.9742
Creo 1067.9742 is a Class II device made by Globus Medical, Inc., cleared under FDA 510(k) K124058 on 13 May 2013 and listed in FDA GUDID since 6 Nov 2015 (UDI-DI 00889095026313), 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 | Number00889095026313 | Date6 Nov 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK124058 | Date13 May 2013 | StatusActive |
Official records
- AccessGUDID record 00889095026313
- FDA 510(k) database K124058
Across registries
- FDA 510(k) K124058 decided 13 May 2013 Active
- FDA GUDID UDI-DI 00889095026313 listed 6 Nov 2015 Listed
Timeline
- Cleared FDA 510(k) K124058
- Listed FDA GUDID 00889095026313
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Creo
- Generic name
- Trans-facet-screw internal spinal fixation system, sterile
- Model / reference
- 1067.9742
- Primary DI / UDI-DI
- 00889095026313
- 510(k) Number
- FDA product code
- OSH, MNH, KWQ, MNI, KWP, NKB
- GMDN term
- Trans-facet-screw internal spinal fixation system, sterile
- Device class
- Class II
- Regulation number
- 888.3070, 888.3060, 888.3050
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- Size
- Height — 11.15 MillimeterWidth — 4.5 Millimeter
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