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VerTouch Spinal Imaging Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN220009
510(k) Type
Direct
Applicant
Intuitap Medical, Inc.
Country
United States
FDA Decision
Deleted
Decision Date
1/19/2024
Days to Decision
717 days

VerTouch Spinal Imaging Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN220009
510(k) Type
Direct
Applicant
Intuitap Medical, Inc.
Country
United States
FDA Decision
Deleted
Decision Date
1/19/2024
Days to Decision
717 days