FDA 510(k) Application Details - DEN220009

Device Classification Name	More FDA Info for this Device
510(K) Number	DEN220009
Device Name	VerTouch Spinal Imaging Device
Applicant	IntuiTap Medical, Inc. 1940 Fountain View Drive Houston, TX 77057 US Other 510(k) Applications for this Company
Contact	Jessica Traver Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QXD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/01/2022
Decision Date	01/19/2024
Decision	DENG -
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status
Type	Direct
Reviewed By Third Party	N
Expedited Review