📋 FDA Reference
Liverty TIPS Stent Graft
Bard Peripheral Vascular, Inc.
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FDA Clearance Information
Pathway ?
PMA
Number ?
P250050 ↗
Decision Date ?
September 25, 2026
Product Code ?
MIR Shunt, Portosystemic, Endoprosthesis
Device Class ?
Class 3
Evidence ?
0 studies
FDA-Cleared Indications
Approval for the Liverty TIPS Stent Graft. The device is indicated for the treatment of complications of portal hypertension
Clinical Applications
Frequently Asked Questions
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Disclaimer: This page compiles publicly available regulatory and published clinical evidence for educational reference.
It does not constitute medical advice, product endorsement, or a recommendation for clinical use.
Always consult manufacturer documentation and clinical judgment for patient care decisions.