Aneurysm Repair Technology Gains FDA Approval


The FDA has granted 510(k) marketing clearance for an endovascular aneurysm repair system (HeliFX, Aptus Endosystems). The device allows for independent endograft fixation. The helical anchor technology is designed to mimic hand suturing performed during open surgical repair.

Source: Aptus Endosystems.

Submit a Comment

Your email address will not be published. Required fields are marked *

9 + 17 =