IceCure Reports Updated Timeline and Progress with FDA Regarding Marketing Authorization for ProSense® Cryoablation in Early-Stage Breast Cancer
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IceCure Medical Ltd. is in ongoing discussions with the FDA for De Novo marketing authorization of its ProSense® cryoablation technology for early-stage breast cancer treatment.
March 20, 2025 | 12:45 pm
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IceCure Medical is actively working with the FDA to obtain De Novo marketing authorization for its ProSense® cryoablation technology, which could significantly impact its market presence in early-stage breast cancer treatment.
The ongoing discussions with the FDA for De Novo marketing authorization are crucial for IceCure's ProSense® technology. Approval would allow IceCure to market its cryoablation technology as an alternative to surgical tumor removal, potentially increasing its market share and revenue. The news is highly relevant and important for investors as it directly affects the company's regulatory progress and future sales potential.
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