← FDA Medical Device Classifications
Optical Neurosurgical Nerve Locator
QWP · Class II — Moderate Risk (510(k) clearance required) · Ear, Nose, Throat · 21 CFR 874.1820
Classification
- FDA Product Code
QWP- Device class
- Class II — Moderate Risk (510(k) clearance required)
- Regulation
- 21 CFR 874.1820
- Review panel
- NE
- Medical specialty
- Ear, Nose, Throat
- Submission type
- 1
- GMP exempt
- N
- Life sustaining
- N
- Implant
- N
- Third-party review
- N
Definition
To locate or monitor function of spinal nerve roots or peripheral nerves during neurosurgery.
Market data
- Cleared 510(k) submissions
- 1
- Registered establishments
- 1
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown