QWP
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Optical Neurosurgical Nerve Locator
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 874.1820
- Medical specialty
- Ear, Nose, Throat
- FDA definition
- To locate or monitor function of spinal nerve roots or peripheral nerves during neurosurgery.
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| Record | Firm | Date |
|---|---|---|
| Waypoint GPS (K222106) | Waypoint Orthopedics, Inc. | 2023-05-12 |
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