Requests that the FDA Warn Women About the Unknown and Inadequately Studied Effect of FDA-Regulated Mesh Devices, Implanted Off-Label in Cosmetic Mastopexy (So-Called “Internal-Bra") Operations, On the Sensitivity of Standard Surveillance Mammography and Ultrasound for Detection of Breast Cancer.
🏛 Food and Drug Administration (FDA)FDA-2023-P-4962
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