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the amplantz goose neck microsnare
Microvena
Summary: The Amplatz Goose Neck Microsnare is a device used for the retrieval of embolic devices and foreign bodies in the vasculature. It is primarily used in endovascular procedures to manage complications such as device migration. Key evidence highlights its efficacy in retrieving detached devices.
FDA Clearance Information
Pathway
510K
Number
K970668 ↗
Decision Date
June 10, 1998
Product Code
DQY
Device Class
Class 2
Evidence
0 studies
The Amplatz Goose Neck Microsnare was cleared by the FDA through the 510(k) pathway on June 10, 1998. It is manufactured by Microvena and classified as a Class 2 medical device.
What It Is
The Amplatz Goose Neck Microsnare is a snare device designed for the retrieval of embolic devices and foreign bodies from the vasculature. It is used in endovascular procedures to address complications such as device migration or malposition.
Clinical Applications
Common clinical scenarios for the Amplatz Goose Neck Microsnare include the retrieval of detached or migrated endovascular devices, such as the Woven EndoBridge (WEB) device, during neurovascular interventions. It is also used in cases of vascular occlusions where foreign body retrieval is necessary.
Evidence Summary
The available literature includes 9 studies, comprising case series and systematic reviews, published between 2021 and 2025. These studies focus on the device's use in retrieving detached devices and managing complications in endovascular procedures.
Reported Outcomes
Published studies report that the Amplatz Goose Neck Microsnare is effective in retrieving detached devices, such as the Woven EndoBridge, with a high success rate. The device has been used successfully in cases of device migration and malposition, demonstrating its utility in complex endovascular procedures.
Safety Profile
Reported complications include rare instances of device malposition and migration, which the Amplatz Goose Neck Microsnare is used to address. The device itself has not been associated with significant adverse events in the reviewed studies.
Evidence Limitations
The evidence is primarily based on case series and systematic reviews, which may limit the generalizability of findings. Further research is needed to evaluate long-term outcomes and safety in larger, more diverse patient populations.
Frequently Asked Questions
What are the clinical indications for Amplatz Goose Neck Microsnare?
The device is indicated for the retrieval of embolic devices and foreign bodies in the vasculature, particularly in cases of device migration or malposition.
What outcomes have been reported in clinical studies?
Studies report successful retrieval of detached devices, such as the Woven EndoBridge, with high efficacy in managing complications.
What complications have been reported?
Reported complications include device malposition and migration, which the Amplatz Goose Neck Microsnare is used to address.
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.