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Wedge XL Delivery Catheter

Page Type
Cleared 510(K)
510(k) Number
K232542
510(k) Type
Traditional
Applicant
MicroVention, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/2024
Days to Decision
268 days
Submission Type
Summary

Wedge XL Delivery Catheter

Page Type
Cleared 510(K)
510(k) Number
K232542
510(k) Type
Traditional
Applicant
MicroVention, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/2024
Days to Decision
268 days
Submission Type
Summary