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U.S. Department of Health and Human Services Food and Drug Administration Center for Devices and Radiological Health Plastic and Reconstructive Surgery Devices Branch Division of General and Restorative Devices Office of Device Evaluation. Guidance for the preparation of a premarket notification application for a surgical mesh. Plastic and reconstructive surgery devices branch; division of general and restorative devices. US Department of Health and Human Services; document shelf number 2247. Available from: http://www.fda.gov/cdrh/index.html; Accessed March 2, 1999.
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