Last synced on 20 December 2024 at 11:05 pm

PreXion3D Explorer PRO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221525
510(k) Type
Traditional
Applicant
PreXion Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
7/22/2022
Days to Decision
57 days
Submission Type
Summary

PreXion3D Explorer PRO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221525
510(k) Type
Traditional
Applicant
PreXion Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
7/22/2022
Days to Decision
57 days
Submission Type
Summary