| Device Type ID | 5208 |
| Device Name | Components, Wheelchair |
| Regulation Description | Wheelchair Component. |
| Regulation Medical Specialty | Physical Medicine |
| Review Panel | Physical Medicine |
| Premarket Review | Office Of Device Evaluation (ODE) Division Of Neurological And Physical Medicine Devices (DNPMD) Physical Medicine And Rehabilitation Devices Branch (PMDB) |
| Submission Type | 510(K) Exempt |
| CFR Regulation Number | 890.3920 [🔎] |
| FDA Device Classification | Class 1 Medical Device |
| Product Code | KNN |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Not Third Party Eligible |
| Device Type ID | 5208 |
| Device | Components, Wheelchair |
| Product Code | KNN |
| FDA Device Classification | Class 1 Medical Device |
| Regulation Description | Wheelchair Component. |
| CFR Regulation Number | 890.3920 [🔎] |
| Device Problems | |
|---|---|
Appropriate Term/Code Not Available | 3 |
Material Integrity Problem | 2 |
Unstable | 1 |
Solder Joint Fracture | 1 |
Adverse Event Without Identified Device Or Use Problem | 1 |
Break | 1 |
Collapse | 1 |
Insufficient Information | 1 |
| Total Device Problems | 11 |