id,agency_id,docket_id,title,document_type,subtype,posted_date,posted_year,posted_month,comment_start_date,comment_end_date,last_modified,fr_doc_num,open_for_comment,withdrawn,object_id
FDA-2002-N-0064-0003,FDA,FDA-2002-N-0064,Neurological Devices; Classification of Human Dura Mater,Notice,Notice of Final Rule,2003-12-18T00:00:00Z,2003,12,2003-12-18T05:00:00Z,,2025-05-13T07:52:58Z,03-31174,0,0,090000648048c4de
FDA-2002-N-0064-0002,FDA,FDA-2002-N-0064,Neurological Devices; Classification of Human Dura Mater,Notice,Notice of Final Rule,2003-12-17T05:00:00Z,2003,12,2003-12-18T05:00:00Z,,2025-05-13T07:51:26Z,03-31174,0,0,090000648048c4db
FDA-2002-N-0064-0001,FDA,FDA-2002-N-0064,Neurological Devices; Classification of Human Dura Mater,Notice,NPR-Notice of Proposed Rule-Making,2002-10-21T04:00:00Z,2002,10,2002-10-22T04:00:00Z,2003-01-22T04:59:59Z,2025-05-13T07:49:19Z,02-26816,0,0,090000648048c4a6