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Medtronic to Begin Feasibility Study of Intrepid TTVR in Heart Valve Disease
Medtronic recently received Breakthrough Device Designation by the FDA for the Intrepid TTVR system.
PR Newswire
09.09.20
Cardiovascular
Surmodics Shares 12-Month Data From Drug-Coated Balloon Early Feasibility Study
Study met primary endpoint and all 12-month secondary safety endpoints including 100 percent freedom from CD-TLR or TVR.
Business Wire
12.18.18
Cardiovascular
PQ Bypass Reports Positive Results for the DETOUR System in Femoropopliteal Artery Blockage
Data show DETOUR System’s ability to successfully treat long blockages without significant impact on venous health.
Business Wire
09.29.17
Cardiovascular
Study Shows Benefit of Endovascular Intervention in Patients With Lower Extremity PAD
Six-month data indicates Cardiovascular Systems' device improves PAD symptoms and quality of life.
Business Wire
02.13.17
R&D & Design
Medtronic Reports Initial Results from Harmony Transcatheter Pulmonary Study
The feasibility study demonstrated positive outcomes in patients at six months.
Medtronic plc
04.05.16
Mitralign Enrolls First Patient in Study of Trialign System
The study will assess the early safety and feasibility of the device, according to the company.
Mitralign Inc.
12.15.15
Breaking News
MPO's Most-Read Stories This Week—April 27
Roivios Receives FDA Breakthrough Device Designation for JuxtaFlow RAD
New CPAP Mask Makes its U.S. Debut
Mike Mathias Joins Endologix as Chief Commercial Officer
Owlstone Medical Gains $6.5M to Develop Breath-Based Diagnostics for Infectious Diseases
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May 2024
Partner Preference in Full-Service Medical Device Outsourcing
Spot Check: A Discussion of the In-Vitro Diagnostics Market
Innovative Iteration for Medical Device Design
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