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StageOne™ Shoulder Cement Spacer Molds

Page Type
Cleared 510(K)
510(k) Number
K221968
510(k) Type
Traditional
Applicant
Biomet, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/2022
Days to Decision
72 days
Submission Type
Summary

StageOne™ Shoulder Cement Spacer Molds

Page Type
Cleared 510(K)
510(k) Number
K221968
510(k) Type
Traditional
Applicant
Biomet, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/2022
Days to Decision
72 days
Submission Type
Summary