Vv-Plug 667145-301
by Oscor Inc.
Vv-Plug 667145-301 is a Class III device made by Oscor Inc., cleared under FDA 510(k) K031164 on 19 Jun 2003 and listed in FDA GUDID since 7 Jul 2016 (UDI-DI 00802526497544), 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 | Number00802526497544 | Date7 Jul 2016 | StatusListed |
| United States | FDA 510(k)ST | NumberK031164 | Date19 Jun 2003 | StatusActive |
Official records
- AccessGUDID record 00802526497544
- FDA 510(k) database K031164
Across registries
- FDA 510(k) K031164 decided 19 Jun 2003 Active
- FDA GUDID UDI-DI 00802526497544 listed 7 Jul 2016 Listed
Timeline
- Cleared FDA 510(k) K031164
- Listed FDA GUDID 00802526497544
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Vv-Plug
- Generic name
- Implantable pulse generator port plug
- Model / Ref / Catalog
- 667145-301, VV-PLUG
- Primary DI / UDI-DI
- 00802526497544
- 510(k) Number
- FDA product code
- DTB
- GMDN term
- Implantable pulse generator port plug
- Device class
- Class III
- Regulation number
- 870.3680
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Implantable pulse generator port plug.