510(k) DEN220009
- Device
- VerTouch Spinal Imaging Device
- Applicant
- Intuitap Medical, Inc.
- 510(k) number
- DEN220009
- Product code
- QXD
- Decision
- Unknown (DENG)
- Decision date
- 2024-01-19
- Date received
- 2022-02-01
- Regulation
- 868.1985
- Classification name
- Spinal Imaging System For Neuraxial Procedures
- Medical specialty
- Anesthesiology
- Review panel
- Anesthesiology
- Device class
- 2
- Clearance type
- Direct
- Third party reviewed
- N
Related Records
Applicant Contact
- Contact
- Jessica Traver
- Address
- 1940 Fountain View Dr. Houston TX US 77057 77057
FDA Registration Numbers
- 3027594726
Source Documents
510(k) summary PDF not indicated by FDA