DEN220009
- 510(k) number
- DEN220009
- Device name
- VerTouch Spinal Imaging Device
- Applicant
- Intuitap Medical, Inc. TX · US
- Product code
- QXD — Spinal Imaging System For Neuraxial Procedures
- Decision date
- 2024-01-19
- Date received
- 2022-02-01
- Decision
- Unknown
- Clearance type
- Direct
- Advisory committee
- Anesthesiology
Official FDA record: DEN220009
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.