Guidant ICD Recalls Spurring High Volume Of Patient Queries, HRS Reports
The Heart Rhythm Society proposes to draft guidance on how doctors should inform patients of device recalls. The document would follow a planned HRS guidance clarifying procedures for ICD manufacturers to report safety alerts to physicians
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A surgeon at Ochsner Health in New Orleans was able to successfully remove a rare and dangerous tumor from a patient’s spine using cutting-edge technology that would have otherwise made the procedure too risky.
The FDA's new Commissioner’s National Priority Voucher program aims to expedite drug approvals significantly. Device firms like XVIVO advocate for a similar initiative for devices, emphasizing the potential for faster reviews and improved patient access to lifesaving technologies.