22017B-Ll
by Medtronic PS Medical 2 variants
22017B-Ll is a Class II device made by Medtronic PS Medical, cleared under FDA 510(k) K873247 on 18 Sep 1987 and listed in FDA GUDID since 8 Jul 2015 (UDI-DI 00643169483606), active as of 22 Oct 2026. One FDA recall is linked to it.
Active
510(k)
Valid until
No expiry
FDA recalls
1 ongoingDocuments
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00643169483606 | Date8 Jul 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK873247 | Date18 Sep 1987 | StatusActive |
Official records
- AccessGUDID record 00643169483606
- FDA 510(k) database K873247
Across registries
- FDA 510(k) K873247 decided 18 Sep 1987 Active
- FDA GUDID UDI-DI 00643169483606 listed 8 Jul 2015 Listed
Recalls
-
- Ongoing Z-1117-2021
Potential for variation in radiopaque marking visibility under radiographic imaging for adjustable and fixed-pressure valves that are used in the management of hydrocephalus
Timeline
- Cleared FDA 510(k) K873247
- Listed FDA GUDID 00643169483606
- Recall initiated FDA recalls Z-1117-2021
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Generic name
- Ventriculoperitoneal shunt
- Model / reference
- 22017B-LL
- Primary DI / UDI-DI
- 00643169483606
- 510(k) Number
- FDA product code
- JXG
- GMDN term
- Ventriculoperitoneal shunt
- Device class
- Class II
- Regulation number
- 882.5550
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 90.0 Centimeter