Cleared Traditional

K241529 - Powered Wheelchair (NXN20-209) (FDA 510(k) Clearance)

Nov 2024
Decision
176d
Days
Class 2
Risk

K241529 is an FDA 510(k) clearance for the Powered Wheelchair (NXN20-209). This device is classified as a Wheelchair, Powered (Class II - Special Controls, product code ITI).

Submitted by Zhejiang Nysin Medical Co., Ltd. (Jinhua, CN). The FDA issued a Cleared decision on November 22, 2024, 176 days after receiving the submission on May 30, 2024.

This device falls under the Physical Medicine FDA review panel. Regulated under 21 CFR 890.3860. A Powered Wheelchair Is A Battery-operated Device With Wheels That Is Intended For Medical Purposes To Provide Mobility To Persons Restricted To A Sitting Position. Fda Interprets “mobility To Persons Restricted To A Sitting Position” To Mean The Device Type Is Intended To Provide Mobility To Individuals Who Have Mobility Impairments And Require An Assistive Device For Mobility. Note: This Type Of Device Is Not Intended To Climb Stairs (see Product Code: Imk)..

Submission Details

510(k) Number K241529 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 30, 2024
Decision Date November 22, 2024
Days to Decision 176 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Summary PDF

Device Classification

Product Code ITI - Wheelchair, Powered
Device Class Class II - Special Controls
CFR Regulation 21 CFR 890.3860
Definition A Powered Wheelchair Is A Battery-operated Device With Wheels That Is Intended For Medical Purposes To Provide Mobility To Persons Restricted To A Sitting Position. Fda Interprets “mobility To Persons Restricted To A Sitting Position” To Mean The Device Type Is Intended To Provide Mobility To Individuals Who Have Mobility Impairments And Require An Assistive Device For Mobility. Note: This Type Of Device Is Not Intended To Climb Stairs (see Product Code: Imk).

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