510(k) clearance
NeuroAlign
- 510(k) number
- K261997
- Applicant
- Medivis, Inc.
- Decision date
- Oct 26, 2026
- Date received
- Jun 15, 2026
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Product code
- HAW
- Device type
- Neurological Stereotaxic Instrument
- Device class
- Class II
- Regulation
- 21 CFR 882.4560
- Advisory committee
- Neurology
- Statement or summary
- Summary
- Third party
- N
- Location
- New York, NY, US