Creo 1200.0720
Active
510(k)
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00889095741773 | Date31 Jul 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK182375 | Date8 Apr 2019 | StatusActive |
Official records
- AccessGUDID record 00889095741773
- FDA 510(k) database K182375
Recalls
No FDA recalls found in the data synced 22 Oct 2026.
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- Withdrawn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
- 1200.0720
- Primary DI / UDI-DI
- 00889095741773
- 510(k) Number
- FDA product code
- KWP, NKB
- GMDN term
- Trans-facet-screw internal spinal fixation system, sterile
- Device class
- Class II
- Regulation number
- 888.3050, 888.3070
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- Size
- Length — 20 Millimeter
Other devices from Globus Medical, Inc.
Properties
Other properties (12)
- Supplied sterile: No
- Implantable: No
- Contains latex: No
- Prescription use: No
- Over-the-counter: No
- Convenience kit: No
- Combination product: No
- HCT/P: No
- Premarket exempt: No
- Serial number: No
- Expiration date: No
- Manufacturing date: No