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withdrawn,object_id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-2019-P-3347-0006,FDA,FDA-2019-P-3347,Medical Devices; Exemption From Premarket Notification; Class II Devices; Powered Wheeled Stretcher,Rule,Final Rule,2020-01-14T05:00:00Z,2020,1,2020-01-14T05:00:00Z,,2020-04-13T16:50:57Z,2020-00295,0,0,090000648429e1b6
FDA-2019-P-3347-0005,FDA,FDA-2019-P-3347,Petition Response Letter from FDA CDRH to Stryker Medical,Other,Agency Response,2020-01-07T05:00:00Z,2020,1,2020-01-07T05:00:00Z,,2020-01-07T15:08:59Z,,0,0,0900006484276af7
FDA-2019-P-3347-0004,FDA,FDA-2019-P-3347,Medical Devices; Exemption From Premarket Notification: Class II; Powered Wheeled Stretcher; Request for Comments,Notice,Announcement,2019-09-16T04:00:00Z,2019,9,2019-09-16T04:00:00Z,2019-11-16T04:59:59Z,2019-09-16T14:16:52Z,2019-19978,0,0,0900006483f6e65a
FDA-2019-P-3347-0003,FDA,FDA-2019-P-3347,"Appendix A MAUDE Database for Product Code INK: May 30, 2014-May 30, 2019 re Citizen Petition from Stryker",Supporting & Related Material,Background Material,2019-07-11T04:00:00Z,2019,7,,,2019-07-11T19:40:58Z,,0,0,0900006483d80544
FDA-2019-P-3347-0002,FDA,FDA-2019-P-3347,Acknowledgment Letter from FDA DDM to Stryker,Other,Acknowledgement Letter/Receipt,2019-07-11T04:00:00Z,2019,7,,,2019-07-11T19:39:41Z,,0,0,0900006483d7e9e9
FDA-2019-P-3347-0001,FDA,FDA-2019-P-3347,Citizen Petition from Stryker,Other,Citizen Petition,2019-07-11T04:00:00Z,2019,7,2019-07-11T04:00:00Z,,2020-01-07T15:09:27Z,,0,0,0900006483d7e444