Uniplate 189706026
Uniplate 189706026 is a Class II device made by Depuy Spine, Inc., cleared under FDA 510(k) K171439 on 20 Jul 2017 (1 earlier submission) and listed in FDA GUDID since 24 Sep 2015 (UDI-DI 10705034180663), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK171439 | Date20 Jul 2017 | StatusActive |
| United States | GUDID listing | Number10705034180663 | Date24 Sep 2015 | StatusListed |
Official records
- AccessGUDID record 10705034180663
- FDA 510(k) database K171439
- FDA 510(k) database K042544
Across registries
- FDA 510(k) K171439 decided 20 Jul 2017 Active
- FDA GUDID UDI-DI 10705034180663 listed 24 Sep 2015 Listed
Timeline
- Cleared FDA 510(k) K042544
- Listed FDA GUDID 10705034180663
- Cleared FDA 510(k) K171439
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Uniplate
- Generic name
- Spinal bone screw, non-bioabsorbable
- Model / Ref / Catalog
- 189706026
- Primary DI / UDI-DI
- 10705034180663
- FDA product code
- KWQ
- GMDN term
- Spinal bone screw, non-bioabsorbable
- Device class
- Class II
- Regulation number
- 888.3060
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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