Mesh 1011152
Mesh 1011152 is a Class II device made by NuVasive, LLC, cleared under FDA 510(k) K023319 on 4 Mar 2003 and listed in FDA GUDID since 24 Oct 2015 (UDI-DI 00887517063922), 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 | Number00887517063922 | Date24 Oct 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK023319 | Date4 Mar 2003 | StatusActive |
Official records
- AccessGUDID record 00887517063922
- FDA 510(k) database K023319
Across registries
- FDA 510(k) K023319 decided 4 Mar 2003 Active
- FDA GUDID UDI-DI 00887517063922 listed 24 Oct 2015 Listed
Timeline
- Cleared FDA 510(k) K023319
- Listed FDA GUDID 00887517063922
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Mesh
- Generic name
- Vertebral body prosthesis
- Model / reference
- 1011152
- Primary DI / UDI-DI
- 00887517063922
- 510(k) Number
- FDA product code
- MQP
- GMDN term
- Vertebral body prosthesis
- 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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- NuVasive PEEK Corpectomy Railed System by Nu Vasive, Incorporated