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withdrawn,object_id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-2022-N-3239-0001,FDA,FDA-2022-N-3239,"Medical Devices; Orthopedic Devices; Classification of the Implantable Post-
Surgical Kinematic Measurement Knee Device",Rule,Final Rule,2023-01-05T05:00:00Z,2023,1,2023-01-05T05:00:00Z,,2023-01-05T14:47:58Z,2022-28604,0,0,090000648558a9d9