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CrossFAST™ Integrated Microcatheter Guide Extension System (CFM55)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242276
510(k) Type
Traditional
Applicant
Vantis Vascular, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/2024
Days to Decision
60 days
Submission Type
Summary

CrossFAST™ Integrated Microcatheter Guide Extension System (CFM55)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242276
510(k) Type
Traditional
Applicant
Vantis Vascular, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/2024
Days to Decision
60 days
Submission Type
Summary