22017B-Ll

by Medtronic PS Medical 2 variants

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

This device is named in the recall

Documents

FDA submission, from GUDID

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00613994908742 UDI-DI	Date17 Jun 2015Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK873247	Date18 Sep 1987Decided	StatusActive

Official records

AccessGUDID record UDI-DI 00613994908742
FDA 510(k) database 510(k) number K873247

Recalls

1 recall · 1 ongoing · FDA

- Ongoing Z-1117-2021 FDA Class II initiated 11 Jan 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

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Generic name: Ventriculoperitoneal shunt
Model / reference: 22017B-LL

Primary DI / UDI-DI: 00613994908742
510(k) Number: K873247
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

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Properties

Supplied sterile
Single use
Implantable
Prescription use
Lot / batch number

Other properties (10)

Sterilise before use: No
Contains latex: No
Over-the-counter: No
Convenience kit: No
Combination product: No
HCT/P: No
Premarket exempt: No
Serial number: No
Expiration date: No
Manufacturing date: No