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VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240578
510(k) Type
Traditional
Applicant
B. Braun Medical Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2024
Days to Decision
152 days
Submission Type
Summary

VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240578
510(k) Type
Traditional
Applicant
B. Braun Medical Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2024
Days to Decision
152 days
Submission Type
Summary