VerTouch Spinal Imaging Device
FDA 510(k) clearance DEN220009 · decided 2024-01-19
Clearance details
- K-number
- DEN220009
- Device name
- VerTouch Spinal Imaging Device
- Applicant
- Intuitap Medical, Inc.
- Decision
- Unknown
- Date received
- 2022-02-01
- Decision date
- 2024-01-19
- Days to decision
- 717 days
- Clearance type
- Direct
- Product code
- QXD
- Device class
- 2
- Regulation number
- 868.1985
- Medical specialty
- Anesthesiology
- Advisory committee
- Anesthesiology
- Location
- Houston, TX, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.