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SmartBase for Arthrex Glenoid IRIS

Page Type
Cleared 510(K)
510(k) Number
K153215
510(k) Type
Traditional
Applicant
Custom Orthopaedic Solutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/2016
Days to Decision
106 days
Submission Type
Summary

SmartBase for Arthrex Glenoid IRIS

Page Type
Cleared 510(K)
510(k) Number
K153215
510(k) Type
Traditional
Applicant
Custom Orthopaedic Solutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/2016
Days to Decision
106 days
Submission Type
Summary