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withdrawn,object_id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-2015-N-3785-0012,FDA,FDA-2015-N-3785,Classification of Posterior Cervical Screw Systems: Small Entity Compliance Guide; Availability,Notice,Notice of Availability,2020-05-04T04:00:00Z,2020,5,2020-05-04T04:00:00Z,,2020-05-04T17:16:54Z,2020-09188,0,0,090000648455007f
FDA-2015-N-3785-0011,FDA,FDA-2015-N-3785,Classification of Posterior Cervical Screw Systems: Small Entity Compliance Guide Guidance for Industry and Food and Drug Administration Staff,Other,Guidance,2020-05-01T04:00:00Z,2020,5,2020-05-01T04:00:00Z,,2024-11-06T23:35:50Z,,1,0,090000648452d524
FDA-2015-N-3785-0010,FDA,FDA-2015-N-3785,Reference 1 for the Final Rule (FRIA) - Medical Devices; Orthopedic Devices; Classification of Posterior Cervical Screw Systems,Other,Additional Information,2019-04-03T04:00:00Z,2019,4,2019-04-03T04:00:00Z,,2019-04-03T14:04:20Z,,0,0,0900006483b5dfbb
FDA-2015-N-3785-0009,FDA,FDA-2015-N-3785,"Medical Devices; Orthopedic Devices; Classification of Posterior Cervical
Screw Systems",Rule,Final Rule,2019-04-01T04:00:00Z,2019,4,2019-04-01T04:00:00Z,,2019-04-01T16:22:28Z,2019-06024,0,0,0900006483b511b1
FDA-2015-N-3785-0008,FDA,FDA-2015-N-3785,"Reference 2 - Transcript and Other Meeting Materials from the FDA Orthopedic Devices Panel Meeting, September 21, 2012  re Medical Devices; Orthopedic Devices; Classification of Posterior Cervical Screw Systems",Supporting & Related Material,Background Material,2018-11-14T05:00:00Z,2018,11,,,2018-11-14T15:25:01Z,,0,0,09000064838d5fc9
FDA-2015-N-3785-0003,FDA,FDA-2015-N-3785,"Reference 2 - Transcript and Other Meeting Materials from the FDA Orthopedic Devices Panel Meeting, September 21, 2012  re Medical Devices; Orthopedic Devices; Classification of Posterior Cervical Screw Systems",Supporting & Related Material,Background Material,2016-03-10T05:00:00Z,2016,3,,,2018-11-14T15:26:33Z,,0,0,0900006481eb80fc
FDA-2015-N-3785-0001,FDA,FDA-2015-N-3785,"Medical Devices; Orthopedic Devices; Classification of Posterior Cervical
Screw Systems",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2016-03-10T05:00:00Z,2016,3,2016-03-10T05:00:00Z,2016-06-09T03:59:59Z,2016-06-09T01:00:36Z,2016-05384,0,0,0900006481eb8198
FDA-2015-N-3785-0002,FDA,FDA-2015-N-3785,Reference 1 - Orthopedic Surgical Manufacturers Association (OSMA) Reclassification Petition - Lateral Mass and Pedicle Screw Spinal Systems (Cervical Spine) re Medical Devices; Orthopedic Devices; Classification of Posterior Cervical Screw Systems,Supporting & Related Material,Background Material,2016-03-10T05:00:00Z,2016,3,,,2016-03-10T21:25:39Z,,0,0,0900006481eb80fb