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withdrawn,object_id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-2010-N-0308-0048,FDA,FDA-2010-N-0308,"Reference 1 - Requests for Feedback on Medical Device Submissions:
The Pre-Submission Program and Meetings with Food and Drug Administration Staff Guidance for Industry and Food and Drug Administration Staff",Supporting & Related Material,Background Material,2016-10-24T04:00:00Z,2016,10,,,2016-10-24T16:05:33Z,,0,0,090000648234481d
FDA-2010-N-0308-0047,FDA,FDA-2010-N-0308,Program for Parallel Review of Medical Devices,Notice,Request for Nominations,2016-10-24T04:00:00Z,2016,10,2016-10-24T04:00:00Z,,2016-10-24T13:54:41Z,2016-25659,0,0,09000064823432a7
FDA-2010-N-0308-0045,FDA,FDA-2010-N-0308,See FDA-2010-N-0308-0046,Notice,General Notice,2013-12-18T05:00:00Z,2013,12,2013-12-18T05:00:00Z,2014-03-04T04:59:59Z,2014-03-09T03:44:59Z,2013-30055,0,0,09000064814c8a96
FDA-2010-N-0308-0046,FDA,FDA-2010-N-0308,Pilot Program for Parallel Review of Medical Products; Extension of the Duration of the Program,Notice,General Notice,2013-12-18T05:00:00Z,2013,12,2013-12-18T05:00:00Z,2014-03-04T04:59:59Z,2014-03-06T21:48:24Z,2013-29822,0,0,09000064814c8999
FDA-2010-N-0308-0044,FDA,FDA-2010-N-0308,Pilot Program for Parallel Review of Medical Products: Correction,Notice,General Notice,2011-10-26T04:00:00Z,2011,10,2011-10-26T04:00:00Z,,2011-10-26T20:45:58Z,2011-27694,0,0,0900006480f5cb51
FDA-2010-N-0308-0043,FDA,FDA-2010-N-0308,Pilot Program for Parallel Review of Medical Products,Notice,General Notice,2011-10-11T04:00:00Z,2011,10,2011-10-11T04:00:00Z,,2012-03-24T19:32:37Z,2011-25907,0,0,0900006480f501bb
FDA-2010-N-0308-0001,FDA,FDA-2010-N-0308,Parallel Review of Medical Products,Notice,N-Notice,2010-09-17T04:00:00Z,2010,9,2010-09-17T04:00:00Z,2010-12-17T04:59:59Z,2010-12-20T20:32:26Z,2010-23252,0,0,0900006480b51dc1