20026 a-M
20026 a-M is a Class II device made by Medtronic PS Medical, cleared under FDA 510(k) K871752 on 22 May 1987 and listed in FDA GUDID since 17 Jun 2015 (UDI-DI 00613994908629), 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 | Number00613994908629 | Date17 Jun 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK871752 | Date22 May 1987 | StatusActive |
Official records
- AccessGUDID record 00613994908629
- AccessGUDID record 00643169497368
- FDA 510(k) database K871752
Across registries
- FDA 510(k) K871752 decided 22 May 1987 Active
- FDA GUDID UDI-DI 00613994908629 listed 17 Jun 2015 Listed
Timeline
- Cleared FDA 510(k) K871752
- Listed FDA GUDID 00613994908629
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Generic name
- Ventriculo-peritoneal/atrial shunt
- Model / reference
- 20026 A-M
- Primary DI / UDI-DI
- 00613994908629, 00643169497368
- 510(k) Number
- FDA product code
- JXG
- GMDN term
- Ventriculo-peritoneal/atrial shunt
- Device class
- Class II
- Regulation number
- 882.5550
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 90.0 CentimeterOuter Diameter — 2.5 Millimeter