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Patient Specific Planning Solution™ 3D Bone Models

Page Type
Cleared 510(K)
510(k) Number
K230540
510(k) Type
Traditional
Applicant
Biomet Manufacturing Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2023
Days to Decision
148 days
Submission Type
Summary

Patient Specific Planning Solution™ 3D Bone Models

Page Type
Cleared 510(K)
510(k) Number
K230540
510(k) Type
Traditional
Applicant
Biomet Manufacturing Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2023
Days to Decision
148 days
Submission Type
Summary