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IntraOp VSP Software Device

Page Type
Cleared 510(K)
510(k) Number
K213128
510(k) Type
Traditional
Applicant
Xironetic, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/2022
Days to Decision
389 days
Submission Type
Summary

IntraOp VSP Software Device

Page Type
Cleared 510(K)
510(k) Number
K213128
510(k) Type
Traditional
Applicant
Xironetic, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/2022
Days to Decision
389 days
Submission Type
Summary