Vu aPod™ - L 31-29-1055
by SeaSpine Orthopedics Corporation
Vu aPod™ - L 31-29-1055 is a Class II device made by SeaSpine Orthopedics Corporation, cleared under FDA 510(k) K112986 on 1 May 2012 and listed in FDA GUDID since 24 Sep 2015 (UDI-DI 10889981047122), 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 | GUDID listing | Number10889981047122 | Date24 Sep 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK112986 | Date1 May 2012 | StatusActive |
Official records
- AccessGUDID record 10889981047122
- FDA 510(k) database K112986
Across registries
- FDA 510(k) K112986 decided 1 May 2012 Active
- FDA GUDID UDI-DI 10889981047122 listed 24 Sep 2015 Listed
Timeline
- Cleared FDA 510(k) K112986
- Listed FDA GUDID 10889981047122
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Vu aPod™ - L
- Generic name
- Vertebral body prosthesis, non-sterile
- Model / Ref / Catalog
- 31-29-1055
- Primary DI / UDI-DI
- 10889981047122
- 510(k) Number
- FDA product code
- MAX, OVD
- GMDN term
- Vertebral body prosthesis, non-sterile
- Device class
- Class II
- Regulation number
- 888.3080
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization