| Device Type ID | 2819 |
| Device Name | Splint, Extremity, Noninflatable, External, Sterile |
| Regulation Description | Noninflatable Extremity Splint. |
| Regulation Medical Specialty | General & Plastic Surgery |
| Review Panel | General Hospital |
| Premarket Review | Office Of Device Evaluation (ODE) Division Of Surgical Devices (DSD) General Surgery Devices Branch One - Light Based/Laser (GSDB1) |
| Submission Type | 510(K) Exempt |
| CFR Regulation Number | 878.3910 [🔎] |
| FDA Device Classification | Class 1 Medical Device |
| Product Code | FYH |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Not Third Party Eligible |
| Device Type ID | 2819 |
| Device | Splint, Extremity, Noninflatable, External, Sterile |
| Product Code | FYH |
| FDA Device Classification | Class 1 Medical Device |
| Regulation Description | Noninflatable Extremity Splint. |
| CFR Regulation Number | 878.3910 [🔎] |
| Device Problems | |
|---|---|
Adverse Event Without Identified Device Or Use Problem | 1 |
| Total Device Problems | 1 |