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PreXion3D Expedition

Page Type
Cleared 510(K)
510(k) Number
K232166
510(k) Type
Traditional
Applicant
PreXion Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
9/8/2023
Days to Decision
49 days
Submission Type
Summary

PreXion3D Expedition

Page Type
Cleared 510(K)
510(k) Number
K232166
510(k) Type
Traditional
Applicant
PreXion Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
9/8/2023
Days to Decision
49 days
Submission Type
Summary