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FDA: Class I Recall for Left-Sided Impella Pumps Due to TAVI Interaction

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FDA: Class I Recall for Left-Sided Impella Pumps Due to TAVI Interaction

July 27, 2023

CMS Issues Proposed Coverage Decision to Broaden Access for Carotid Stenting

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CMS Issues Proposed Coverage Decision to Broaden Access for Carotid Stenting

July 12, 2023

FDA: All Restrictions on Paclitaxel Devices for PAD Are Removed

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FDA: All Restrictions on Paclitaxel Devices for PAD Are Removed

July 11, 2023

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