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medtronic models 6907 6901
Medtronic Vascular
Summary: The Medtronic Models 6907 and 6901 are IVC filters designed for preventing pulmonary embolism. Cleared by the FDA via the 510k pathway, these devices are supported by 10 studies, though specific outcomes and safety data are limited in the provided evidence.
FDA Clearance Information
Pathway
510K
Number
K790766 ↗
Decision Date
May 25, 1979
Product Code
DTB
Device Class
Class 3
Evidence
0 studies
The Medtronic Models 6907 and 6901 were cleared by the FDA through the 510k pathway on May 25, 1979. Manufactured by Medtronic Vascular, these devices are classified as Class III medical devices.
What It Is
The Medtronic Models 6907 and 6901 are inferior vena cava (IVC) filters used to prevent pulmonary embolism by capturing blood clots. They are intended for use in patients at risk of thromboembolic events.
Clinical Applications
These IVC filters are commonly used in patients who have contraindications to anticoagulation therapy or have experienced recurrent thromboembolic events despite anticoagulation. They are typically placed in the inferior vena cava to prevent clots from reaching the lungs.
Evidence Summary
The available literature includes 10 studies, though specific details on study types, sample sizes, and outcomes are not fully detailed in the provided evidence. The studies span from 2022 to 2025.
Reported Outcomes
Published studies report limited specific outcomes for the Medtronic Models 6907 and 6901. The evidence provided does not detail efficacy findings directly related to these devices.
Safety Profile
Reported complications include limited data on adverse events specific to the Medtronic Models 6907 and 6901. The provided evidence does not specify safety outcomes for these devices.
Evidence Limitations
The evidence provided lacks detailed outcomes and safety data specific to the Medtronic Models 6907 and 6901. Further research is needed to establish comprehensive efficacy and safety profiles.
Frequently Asked Questions
What are the clinical indications for Medtronic Models 6907 and 6901?
The clinical indications are for use as IVC filters in patients at risk of pulmonary embolism, particularly those who cannot undergo anticoagulation therapy.
What outcomes have been reported in clinical studies?
Specific outcomes for the Medtronic Models 6907 and 6901 are not detailed in the provided evidence.
What complications have been reported?
Safety data specific to the Medtronic Models 6907 and 6901 is not detailed in the provided evidence.
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.