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Arthrex OrthoVis Preoperative Plan

Page Type
Cleared 510(K)
510(k) Number
K151568
510(k) Type
Traditional
Applicant
Custom Orthopaedic Solutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2015
Days to Decision
51 days
Submission Type
Summary

Arthrex OrthoVis Preoperative Plan

Page Type
Cleared 510(K)
510(k) Number
K151568
510(k) Type
Traditional
Applicant
Custom Orthopaedic Solutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2015
Days to Decision
51 days
Submission Type
Summary