QXM · Implanted Tibial Electrical Urinary Continence Device

Gastroenterology, Urology · 21 CFR 876.5305 · Class 2

Overview

Product CodeQXM
Device NameImplanted Tibial Electrical Urinary Continence Device
Regulation21 CFR 876.5305
Device ClassClass 2
Review PanelGastroenterology, Urology
ImplantYes

Identification

An implanted tibial electrical urinary continence device is an implanted prescription device that receives power from a non-implanted external power source to provide electrical stimulation of the tibial nerve in proximity to the ankle. The device is intended for the treatment of overactive bladder related symptoms of urge urinary incontinence, urinary urgency, urinary frequency and nocturia.

Classification Rationale

Class II (special controls). The device is classified as Class II because the probable benefits outweigh the probable risks, and the risks can be mitigated by the use of general and the identified special controls.

Special Controls

In combination with the general controls of the FD&C Act, an implanted tibial electrical urinary continence device is subject to the following special controls:

Recent Cleared Devices (3 of 3)

RecordDevice NameApplicantDecision DateDecision
K252391Revi SystemBluewind Medical , Ltd.Dec 12, 2025SESE
K240037Revi™ SystemBluewind Medical , Ltd.May 2, 2024SESE
DEN220073Revi SystemBluewind Medical , Ltd.Aug 16, 2023DENG

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