federal_register: 2011-15817

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document_number title type abstract publication_date pub_year pub_month html_url pdf_url agency_names agency_ids excerpts
2011-15817 Medical Devices; Neurological Devices; Clarification of Classification for Human Dura Mater; Technical Amendment Rule The Food and Drug Administration (FDA) is amending the device regulations to clarify the applicability of the device classification for human dura mater. This action is being taken to improve the accuracy of the regulations. 2011-06-24 2011 6 https://www.federalregister.gov/documents/2011/06/24/2011-15817/medical-devices-neurological-devices-clarification-of-classification-for-human-dura-mater-technical https://www.govinfo.gov/content/pkg/FR-2011-06-24/pdf/2011-15817.pdf Health and Human Services Department; Food and Drug Administration 221,199 The Food and Drug Administration (FDA) is amending the device regulations to clarify the applicability of the device classification for human dura mater. This action is being taken to improve the accuracy of the regulations.

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