Orchestra BioMed’s Hypertension Device Wins FDA Breakthrough Designation
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7 Articles
Orchestra BioMed’s Hypertension Device Wins FDA Breakthrough Designation
Orchestra BioMed’s hypertension treatment is the latest medical device to earn the FDA’s breakthrough designation. Medtronic has a commercialization deal with the company for the device, which uses a pacing algorithm to actively lower blood pressure in people with pacemakers. The post Orchestra BioMed’s Hypertension Device Wins FDA Breakthrough Designation appeared first on MedCity News.
Orchestra BioMed receives Breakthrough Device Designation for its hypertension therapy
The company received the designation for its atrioventricular interval modulation therapy, a novel pacemaker-based treatment aimed at reducing blood pressure in patients with uncontrolled hypertension and elevated cardiovascular risk.
Pacemaker to control BP gets FDA nod - Juta MedicalBrief
The US Food and Drug Administration (FDA) has given Breakthrough Device Designation to Orchestra BioMed for its atrioventricular interval modulation (AVIM) therapy for patients with uncontrolled hypertension. AVIM is a pacing algorithm incorporated into dual-chamber pacemakers to treat hypertension. It delivers repeating sequences of shorter and longer atrioventricular delays, lowering blood pressure while simultaneously modulating the autonomic…
Orchestra BioMed to Highlight Advancements in Cardiac Therapy at HRS 2025
NEW HOPE, PA — Orchestra BioMed Holdings, Inc. (Nasdaq: OBIO) will host a satellite symposium at the Heart Rhythm Society (HRS) 2025 Annual Meeting in San Diego to spotlight its atrioventricular interval modulation (AVIM) therapy. The event, scheduled for April 25, will discuss the therapy’s potential to address hypertension in patients at increased cardiovascular risk. The symposium follows the U.S. Food and Drug Administration’s recent grantin…
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