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PreXion3D Explorer

Page Type
Cleared 510(K)
510(k) Number
K190320
510(k) Type
Traditional
Applicant
PreXion Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
4/15/2019
Days to Decision
61 days
Submission Type
Summary

PreXion3D Explorer

Page Type
Cleared 510(K)
510(k) Number
K190320
510(k) Type
Traditional
Applicant
PreXion Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
4/15/2019
Days to Decision
61 days
Submission Type
Summary