Endoskeleton TAS 2312-0111
Endoskeleton TAS 2312-0111 is a Class II device made by Titan Spine, Inc., cleared under FDA 510(k) K111626 on 9 Sep 2011 and listed in FDA GUDID since 17 Sep 2015 (UDI-DI M682231201110), active (FDA 510(k)), not in commercial distribution (GUDID) 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 | GUDID listing | NumberM682231201110 | Date17 Sep 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK111626 | Date9 Sep 2011 | StatusActive |
Official records
- FDA 510(k) database K111626
Across registries
- FDA 510(k) K111626 decided 9 Sep 2011 Active
- FDA GUDID UDI-DI M682231201110 listed 17 Sep 2015 Listed
Timeline
- Cleared FDA 510(k) K111626
- Listed FDA GUDID M682231201110
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Endoskeleton TAS
- Generic name
- Metallic spinal interbody fusion cage
- Model / Ref / Catalog
- 2312-0111
- Primary DI / UDI-DI
- M682231201110
- 510(k) Number
- FDA product code
- OVD
- GMDN term
- Metallic spinal interbody fusion cage
- Device class
- Class II
- Regulation number
- 888.3080
- GUDID distribution status
- Not in Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- Size
- Height — 11 MillimeterDepth — 21 MillimeterWidth — 32 MillimeterAngle — 12 degree
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