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withdrawn,object_id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-2006-N-0178-0056,FDA,FDA-2006-N-0178,Stay of Action Petition Response to Ferrosan A/S from FDA CDRH,Other,Response(s),2021-09-28T04:00:00Z,2021,9,2021-09-28T04:00:00Z,,2021-09-28T13:54:36Z,,0,0,0900006484dae704
FDA-2006-N-0178-0049,FDA,FDA-2006-N-0178,General and Plastic Surgery Devices; Reclassification of the Absorbable Hemostatic Device; Reopening of Comment Period,Proposed Rule,NEC-Notice of Extension,2008-09-11T04:00:00Z,2008,9,2008-09-11T04:00:00Z,2008-10-15T03:59:59Z,2024-11-12T04:19:46Z,E8-21200,1,0,09000064806ff307
FDA-2006-N-0178-0050,FDA,FDA-2006-N-0178,Go to Docket FDA-2006-D-0356 to comment on Draft Guidance for Industry and Food and Drug Administration Staff; Class II Special Controls Guidance Document: Absorbable Hemostatic Device; Availability; Reopening of Comment Period,Notice,NEC-Notice of Extension,2008-09-11T04:00:00Z,2008,9,2008-09-11T04:00:00Z,,2008-09-11T12:56:34Z,,0,0,09000064806ff5bc
FDA-2006-N-0178-0010,FDA,FDA-2006-N-0178,"Ethicon, Inc. - Request for Extension Comment Due Date",Other,EXT-Request for Extension Comment Due Date,2008-07-07T04:00:00Z,2008,7,2008-07-07T04:00:00Z,,2013-07-27T20:44:09Z,,0,0,0900006480450ba0
FDA-2006-N-0178-0009,FDA,FDA-2006-N-0178,"Ethicon, Inc. - Request for Extension Comment Due Date",Other,EXT-Request for Extension Comment Due Date,2008-07-07T04:00:00Z,2008,7,2008-07-07T04:00:00Z,,2013-07-27T20:44:09Z,,0,0,0900006480450b9f
FDA-2006-N-0178-0008,FDA,FDA-2006-N-0178,Ferrosan A/S - Request for Extension Comment Due Date,Other,EXT-Request for Extension Comment Due Date,2008-07-07T04:00:00Z,2008,7,2008-07-07T04:00:00Z,,2013-07-27T20:44:09Z,,0,0,0900006480450b9d
FDA-2006-N-0178-0007,FDA,FDA-2006-N-0178,Ferrosan A/S - Citizen Petition,Other,CP-Citizen Petition,2008-07-07T04:00:00Z,2008,7,2008-07-07T04:00:00Z,,2008-07-07T18:13:02Z,,0,0,0900006480450bd8
FDA-2006-N-0178-0046,FDA,FDA-2006-N-0178,Tab 1 - FDA Center for Devices and Radiological Health - Background Material,Supporting & Related Material,BKG-Background Material,2008-07-07T04:00:00Z,2008,7,,,2008-07-07T23:35:07Z,,0,0,0900006480450bdc
FDA-2006-N-0178-0048,FDA,FDA-2006-N-0178,Tab 3 - FDA Center for Devices and Radiological Health - Background Material,Supporting & Related Material,BKG-Background Material,2008-07-07T04:00:00Z,2008,7,,,2008-07-07T23:35:09Z,,0,0,0900006480450bdf
FDA-2006-N-0178-0047,FDA,FDA-2006-N-0178,Tab 2 - FDA Center for Devices and Radiological Health - Background Material,Supporting & Related Material,BKG-Background Material,2008-07-07T04:00:00Z,2008,7,,,2008-07-07T23:35:08Z,,0,0,0900006480450bde
FDA-2006-N-0178-0045,FDA,FDA-2006-N-0178,FDA Center for Devices and Radiological Health - Background Material,Supporting & Related Material,BKG-Background Material,2008-07-07T04:00:00Z,2008,7,,,2008-07-07T23:30:43Z,,0,0,0900006480450bdd
FDA-2006-N-0178-0006,FDA,FDA-2006-N-0178,Acknowledgement Letter to DuVal & Associates[on Behalf of Ferrosan A/S],Other,ACK-Acknowledgement Letter,2007-07-09T04:00:00Z,2007,7,,,2008-07-07T18:14:28Z,,0,0,0900006480450bda
FDA-2006-N-0178-0005,FDA,FDA-2006-N-0178,General and Plastic Surgery Devices; Reclassification of the Absorbable Hemostatic Device; Reopening of Comment Period,Proposed Rule,NEC-Notice of Extension,2007-05-09T04:00:00Z,2007,5,2007-05-07T04:00:00Z,2007-06-08T03:59:59Z,2008-07-07T18:17:28Z,,0,0,0900006480450bb4
FDA-2006-N-0178-0002,FDA,FDA-2006-N-0178,Reference,Supporting & Related Material,REF-Reference (internal unless indicated),2006-10-31T05:00:00Z,2006,10,,,2008-04-11T23:10:00Z,,0,0,0900006480450b94
FDA-2006-N-0178-0004,FDA,FDA-2006-N-0178,Reference,Supporting & Related Material,REF-Reference (internal unless indicated),2006-10-31T05:00:00Z,2006,10,,,2008-04-11T23:10:00Z,,0,0,0900006480450b9c
FDA-2006-N-0178-0001,FDA,FDA-2006-N-0178,General and Plastic Surgery Devices; Reclassification of the Absorbable Hemostatic Device,Proposed Rule,NPR-Notice of Proposed Rule-Making,2006-10-31T05:00:00Z,2006,10,2006-10-30T05:00:00Z,2007-01-30T04:59:59Z,2008-07-07T18:20:13Z,,0,0,0900006480450b90
FDA-2006-N-0178-0003,FDA,FDA-2006-N-0178,Reference,Supporting & Related Material,REF-Reference (internal unless indicated),2006-10-31T05:00:00Z,2006,10,,,2008-04-11T23:10:00Z,,0,0,0900006480450b9b