VerTouch Spinal Imaging Device— 510(k) DEN220009
UnknownIntuitap Medical, Inc.
FDA 510(k) clearance DEN220009 for VerTouch Spinal Imaging Device, Unknown on 2024-01-19. Applicant: Intuitap Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Intuitap Medical, Inc.
- Product code
- Code QXD
- Device class
- Class 2
- Regulation
- 21 CFR 868.1985
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Houston, TX, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.