Icecure medical announced today that the fda granted marketing authorization for its prosense cryoablation system for breast cancer. The fda’s decision was informed by data from icecure’s ice3 trial involving 194 patients aged 60 and above, published in the annals of surgical oncology Israel’s icecure medical, developer of a minimally invasive system that destroys cancerous tumors by freezing them with liquid nitrogen, announced that the u.s
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Food and drug administration (fda) has granted marketing authorization for its prosense cryoablation system to treat breast cancer.
