Submission Details
| 510(k) Number | K241529 FDA.gov |
| FDA Decision | Cleared 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 |
K241529 is an FDA 510(k) clearance for the Powered Wheelchair (NXN20-209), 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 review panel. Regulated under 21 CFR 890.3860.
| 510(k) Number | K241529 FDA.gov |
| FDA Decision | Cleared 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 |
| 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). |