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AGILON® XO Shoulder Replacement System

Page Type
Cleared 510(K)
510(k) Number
K231657
510(k) Type
Traditional
Applicant
Implantcast, GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
2/16/2024
Days to Decision
254 days
Submission Type
Summary

AGILON® XO Shoulder Replacement System

Page Type
Cleared 510(K)
510(k) Number
K231657
510(k) Type
Traditional
Applicant
Implantcast, GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
2/16/2024
Days to Decision
254 days
Submission Type
Summary