Last synced on 20 December 2024 at 11:05 pm

IntraOp VSP Software Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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