Immediately following the receipt of the NSE letter and through today, HeartBeam has been engaging with the Food and Drug Administration (FDA) review staff to better understand the concerns and determine the best path forward.

• The FDA has signaled a willingness to work with the Company towards a constructive resolution.
• The Company stands behind the clinical study (VALID-ECG) submitted in support of the application. The study met its clinical endpoints and the Company believes it has a viable argument to address outstanding concerns of the agency.
• The Company believes these concerns can be addressed through modifications to the proposed labeling of the device.

HeartBeam has determined that the best course of action to reach a favorable resolution with the FDA is to pursue multiple parallel paths, which are designed for this type of situation.

• The range of options include, but are not limited to, an appeal process or a resubmission of a 510(k) application.
• Based on the recent discussions with the FDA and the information available at present, the Company believes there is a path forward under an appeal process.
• The official appeal process has a timeline of approximately 60 days from submission of an appeal to resolution.

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