CVRx, Inc. announced recently that the Centers for Medicare and Medicaid Services (CMS) assigned the company’s Barostim p ...
Akura Medical, a Shifamed portfolio company focused on venous thromboembolism care, announced recently that the FDA has approve ...
A nationwide retrospective study evaluated health care resource utilization and outcomes among patients with intermediate-risk ...
Medtronic and Recor Medical, Inc. (and its parent company, Otsuka Medical Devices Co., Ltd.) separately and independently ...
Two-year outcomes were reported from the CLOUT registry, which is a prospective, multicenter study evaluating patient ...
DEEPER OUS is a prospective, nonrandomized, multicenter, single-arm trial taking place in New Zealand, Germany, and Switzerland ...
A study assessed the effects of intravascular volume expansion on deep pelvic vein size using the 200-150-125 rule for the ...
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 ...
Findings were presented from the international PEERLESS randomized controlled trial comparing patient outcomes after ...
In the LIFE-BTK trial, several initiatives were implemented to facilitate enrollment of diverse populations, ensuring that pati ...
The ELEGANCE registry, which is focused on historically underrepresented minorities and women, analyzed endovascular treatment ...