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Arthrex Glenoid Intelligent Reusable Instrument System, Arthrex OrthoVis Preoperative Plan, SmartBase for Arthrex Glenoid IRIS, ArthrexVIP Web Portal

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162697
510(k) Type
Traditional
Applicant
Custom Orthopaedic Solutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/2017
Days to Decision
136 days
Submission Type
Summary

Arthrex Glenoid Intelligent Reusable Instrument System, Arthrex OrthoVis Preoperative Plan, SmartBase for Arthrex Glenoid IRIS, ArthrexVIP Web Portal

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162697
510(k) Type
Traditional
Applicant
Custom Orthopaedic Solutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/2017
Days to Decision
136 days
Submission Type
Summary