Last synced on 14 November 2025 at 11:06 pm

Orthoscan VERSA Mini C-Arm

Page Type
Cleared 510(K)
510(k) Number
K243452
510(k) Type
Traditional
Applicant
Ziehm-Orthoscan, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/14/2025
Days to Decision
68 days
Submission Type
Summary

Orthoscan VERSA Mini C-Arm

Page Type
Cleared 510(K)
510(k) Number
K243452
510(k) Type
Traditional
Applicant
Ziehm-Orthoscan, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/14/2025
Days to Decision
68 days
Submission Type
Summary