CVRx, Inc. announced recently that the Centers for Medicare and Medicaid Services (CMS) assigned the company’s Barostim p ...
Two-year outcomes from the PROMISE II trial assessed transcatheter arterialization of the deep veins (TADV) using the LimFlow S ...
Akura Medical, a Shifamed portfolio company focused on venous thromboembolism care, announced recently that the FDA has approve ...
Medtronic and Recor Medical, Inc. (and its parent company, Otsuka Medical Devices Co., Ltd.) separately and independently ...
A nationwide retrospective study evaluated health care resource utilization and outcomes among patients with intermediate-risk ...
Two-year outcomes were reported from the CLOUT registry, which is a prospective, multicenter study evaluating patient outcomes ...
A study assessed the effects of intravascular volume expansion on deep pelvic vein size using the 200-150-125 rule for the ...
DEEPER OUS is a prospective, nonrandomized, multicenter, single-arm trial taking place in New Zealand, Germany, and Switzerland ...
Secondary outcomes through 6 months were reported from the VenaSeal Spectrum Surgical Stripping study, a randomized ...
The final results from the DETOUR2 study evaluated the durability of percutaneous transmural arterial bypass (PTAB) using the D ...
The prospective, multicenter ROADSTER 3 postapproval trial is evaluating the safety and effectiveness of transcarotid artery re ...
Royal Philips announced enrollment of the first patient in THOR, a United States investigational device exemption (IDE) clinica ...