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Elixir Medical has announced it has been granted Breakthrough Device Designation by the U.S. Food and Drug Administration (FDA) for its DynamX BTK System, a novel, adaptive implant for use in the treatment of narrowed or blocked vessels below-the-knee (BTK) in patients with chronic limb-threatening ischemia (CLTI). The company reports this broadens the use of the novel bioadaptor platform technology beyond the treatment of coronary artery disease.

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Motasim Sirhan ,Drug Administration ,Elixir Medical ,Breakthrough Device Designation ,Dynamx Bioadaptor ,Device Designation ,United Kingdom ,

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