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The LimFlow System provides a minimally invasive endovascular solution for patients with end-stage CLTI who have exhausted all other treatment options. The system uses percutaneous deep vein arterialization to bypass blocked arteries and restore blood flow to the ischemic foot. Clinical results from pivotal trials such as PROMISE II demonstrated that the device can save most patients from major amputation, promote wound healing, relieve pain, and improve quality of life. The technology received FDA approval in the US in 2023 after earlier CE Mark approval in Europe
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