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AGILON XO Shoulder System

Page Type
Cleared 510(K)
510(k) Number
K222482
510(k) Type
Traditional
Applicant
Implantcast, GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
9/28/2022
Days to Decision
42 days
Submission Type
Summary

AGILON XO Shoulder System

Page Type
Cleared 510(K)
510(k) Number
K222482
510(k) Type
Traditional
Applicant
Implantcast, GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
9/28/2022
Days to Decision
42 days
Submission Type
Summary