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Arthrex Virtual Implant Positioning (VIP) System

Page Type
Cleared 510(K)
510(k) Number
K230904
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/2023
Days to Decision
83 days
Submission Type
Summary

Arthrex Virtual Implant Positioning (VIP) System

Page Type
Cleared 510(K)
510(k) Number
K230904
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/2023
Days to Decision
83 days
Submission Type
Summary