VisCardia

VisCardia

医疗设备

Beaverton,OR 341 位关注者

We don’t make a weak heart work harder, we make it easier for the weak heart to work

关于我们

VisCardia Inc is a privately held medical device company in Portland Oregon developing a novel chronic heart failure therapy. The VisOne implantable system delivers Synchronized Diaphragmatic Stimulation (SDS) which generates transient intrathoracic pulses gaited to cardiac activity and augments cardiac hemodynamics.

网站
https://www.viscardia.com
所属行业
医疗设备
规模
2-10 人
总部
Beaverton,OR
类型
私人持股
创立
2015
领域
Medical Devices和Heart Failure

地点

  • 主要

    Creekside Corporate Park

    8770 SW Nimbus Ave

    US,OR,Beaverton,97008

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VisCardia员工

动态

  • VisCardia转发了

    查看VisCardia的公司主页,图片

    341 位关注者

    CMS Agrees With VisCardia on the Value of Synchronized Diaphragmatic Stimulation #heartfailure #SDS #HFrEF #viscardia #IDE #CMS #RECOVERHF PORTLAND, OR November 5, 2024 EINPresswire.com VisCardia, Inc. announced today that they have received payment assignments for the designated CPT III codes for VisONE SDS? therapy by the Centers for Medicare and Medicaid Services (CMS). These payment assignments were created subsequently to the FDA approval of the RECOVER-HF clinical trial for the VisONE SDS system as a category B device and related services. The primary CPT code previously designated by the American Medical Association for the VisONE SDS system implantation has been assigned to APC 5465 which carries an average payment rate of over $30,000 in the CY 2025 OPPS Final Rule. Peter Bauer, Ph.D., CEO of VisCardia, expressed his excitement regarding this latest milestone, “We would like to express our thanks to CMS for recognizing the value of this Breakthrough Technology that represents a minimally-invasive, alternative for the treatment of heart failure with reduced ejection fraction (HFrEF) in patients who remain symptomatic on medical therapy and are ineligible for cardiac resynchronization therapy.” The reimbursement rule is effective January 1, 2025. With both FDA and CMS approvals for the pivotal clinical trial, RECOVER-HF, VisCardia is now recruiting clinical sites to help bring this innovative technology to the U.S. market with first U.S. implants anticipated in Q1 2025. In contrast to other device-based heart failure therapies, minimally-invasive Synchronized Diaphragmatic Stimulation? (SDS) allows for a wide access to the healthcare system through outpatient procedures not limited to transplant centers, cardiac surgery centers, other subspecialty surgical suites or even interventional cardiology laboratories. Once approved, the VisONE SDS system will be able to be implanted in basically any surgical suite in a hospital or ambulatory surgical center currently performing laparoscopic procedures or over 30,000 facilities nationwide. Dr. Michael Mirro, Director of Medical Affairs, stated, “The minimally-invasive implant technique lends itself perfectly as an outpatient procedure utilizing facilities that are less congested with high volumes or long procedure times such as cardiac catheterization/EP labs or high acuity surgical suites.” About VisONE? SDS? Therapy The VisONE implantable system delivers VisCardia's proprietary Synchronized Diaphragmatic Stimulation (SDS) therapy for improving cardiac function in heart failure patients. By electrically stimulating the diaphragm in an imperceptible manner, transient intrathoracic pressures synchronized to cardiac activity are modulated, improving both cardiac filling and output. The therapy is non-invasively adjusted and programmed using an external programmer to improve hemodynamic benefit and optimize stimulation parameters. Gregg Harris VisCardia Inc. [email protected]

  • 查看VisCardia的公司主页,图片

    341 位关注者

    CMS Agrees With VisCardia on the Value of Synchronized Diaphragmatic Stimulation #heartfailure #SDS #HFrEF #viscardia #IDE #CMS #RECOVERHF PORTLAND, OR November 5, 2024 EINPresswire.com VisCardia, Inc. announced today that they have received payment assignments for the designated CPT III codes for VisONE SDS? therapy by the Centers for Medicare and Medicaid Services (CMS). These payment assignments were created subsequently to the FDA approval of the RECOVER-HF clinical trial for the VisONE SDS system as a category B device and related services. The primary CPT code previously designated by the American Medical Association for the VisONE SDS system implantation has been assigned to APC 5465 which carries an average payment rate of over $30,000 in the CY 2025 OPPS Final Rule. Peter Bauer, Ph.D., CEO of VisCardia, expressed his excitement regarding this latest milestone, “We would like to express our thanks to CMS for recognizing the value of this Breakthrough Technology that represents a minimally-invasive, alternative for the treatment of heart failure with reduced ejection fraction (HFrEF) in patients who remain symptomatic on medical therapy and are ineligible for cardiac resynchronization therapy.” The reimbursement rule is effective January 1, 2025. With both FDA and CMS approvals for the pivotal clinical trial, RECOVER-HF, VisCardia is now recruiting clinical sites to help bring this innovative technology to the U.S. market with first U.S. implants anticipated in Q1 2025. In contrast to other device-based heart failure therapies, minimally-invasive Synchronized Diaphragmatic Stimulation? (SDS) allows for a wide access to the healthcare system through outpatient procedures not limited to transplant centers, cardiac surgery centers, other subspecialty surgical suites or even interventional cardiology laboratories. Once approved, the VisONE SDS system will be able to be implanted in basically any surgical suite in a hospital or ambulatory surgical center currently performing laparoscopic procedures or over 30,000 facilities nationwide. Dr. Michael Mirro, Director of Medical Affairs, stated, “The minimally-invasive implant technique lends itself perfectly as an outpatient procedure utilizing facilities that are less congested with high volumes or long procedure times such as cardiac catheterization/EP labs or high acuity surgical suites.” About VisONE? SDS? Therapy The VisONE implantable system delivers VisCardia's proprietary Synchronized Diaphragmatic Stimulation (SDS) therapy for improving cardiac function in heart failure patients. By electrically stimulating the diaphragm in an imperceptible manner, transient intrathoracic pressures synchronized to cardiac activity are modulated, improving both cardiac filling and output. The therapy is non-invasively adjusted and programmed using an external programmer to improve hemodynamic benefit and optimize stimulation parameters. Gregg Harris VisCardia Inc. [email protected]

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融资

VisCardia 共 2 轮

上一轮

B 轮

US$12,500,000.00

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