Novus™ NL8509321
Novus™ NL8509321 is a Class II device made by Integra Lifesciences Corp., cleared under FDA 510(k) K153041 on 14 Mar 2016 (1 earlier submission) and listed in FDA GUDID since 22 Sep 2015 (UDI-DI 10381780071761), 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 | NumberK153041 | Date14 Mar 2016 | StatusActive |
| United States | GUDID listing | Number10381780071761 | Date22 Sep 2015 | StatusListed |
Official records
- AccessGUDID record 10381780071761
- FDA 510(k) database K153041
- FDA 510(k) database K961859
Across registries
- FDA 510(k) K153041 decided 14 Mar 2016 Active
- FDA GUDID UDI-DI 10381780071761 listed 22 Sep 2015 Listed
Timeline
- Cleared FDA 510(k) K961859
- Listed FDA GUDID 10381780071761
- Cleared FDA 510(k) K153041
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Novus™
- Generic name
- Ventriculoperitoneal shunt
- Model / Ref / Catalog
- NL8509321
- Primary DI / UDI-DI
- 10381780071761
- FDA product code
- JXG
- GMDN term
- Ventriculoperitoneal shunt
- Device class
- Class II
- Regulation number
- 882.5550
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional