documents
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
8 rows where docket_id = "FDA-2017-N-6730" and posted_year = 2017 sorted by posted_date descending
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Suggested facets: subtype, last_modified, posted_date (date), comment_start_date (date), comment_end_date (date), last_modified (date)
| 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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-2017-N-6730-0007 | FDA | None FDA-2017-N-6730 | Ref. 1, FDA, Medical Device Reporting--Alternative Summary Reporting (ASR) Program Guidance for Industry | Supporting & Related Material | Background Material | 2017-12-26T05:00:00Z | 2017 | 12 | 2017-12-26T17:58:17Z | 0 | 0 | 0900006482d737cd | |||
| FDA-2017-N-6730-0004 | FDA | None FDA-2017-N-6730 | Ref. 4, MDUFA IV Performance Goals and Procedures. Fiscal Years 2019 through 2022 Commitment Letter | Supporting & Related Material | Background Material | 2017-12-26T05:00:00Z | 2017 | 12 | 2017-12-26T17:58:17Z | 0 | 0 | 0900006482d737d0 | |||
| FDA-2017-N-6730-0002 | FDA | None FDA-2017-N-6730 | Ref. 6, Food and Drug Administration, Electronic Medical Device Reporting | Supporting & Related Material | Background Material | 2017-12-26T05:00:00Z | 2017 | 12 | 2017-12-26T17:58:16Z | 0 | 0 | 0900006482d73945 | |||
| FDA-2017-N-6730-0008 | FDA | None FDA-2017-N-6730 | List of References - Voluntary Malfunction Summary Reporting Program fro Manufacturers | Supporting & Related Material | Background Material | 2017-12-26T05:00:00Z | 2017 | 12 | 2017-12-26T17:58:17Z | 0 | 0 | 0900006482d737cb | |||
| FDA-2017-N-6730-0005 | FDA | None FDA-2017-N-6730 | Ref. 3, FDA Form 3500A - MEDWATCH | Supporting & Related Material | Background Material | 2017-12-26T05:00:00Z | 2017 | 12 | 2017-12-26T17:58:17Z | 0 | 0 | 0900006482d737cf | |||
| FDA-2017-N-6730-0003 | FDA | None FDA-2017-N-6730 | Ref. 5, Appedix A, Case Examples of Summary Malfunction Reporting | Supporting & Related Material | Background Material | 2017-12-26T05:00:00Z | 2017 | 12 | 2017-12-26T17:58:17Z | 0 | 0 | 0900006482d737d1 | |||
| FDA-2017-N-6730-0006 | FDA | None FDA-2017-N-6730 | Ref. 2, Food and Drug Administration, MDR Adverse Event Codes | Supporting & Related Material | Background Material | 2017-12-26T05:00:00Z | 2017 | 12 | 2017-12-26T17:58:17Z | 0 | 0 | 0900006482d737ce | |||
| FDA-2017-N-6730-0001 | FDA | None FDA-2017-N-6730 | Center for Devices and Radiological Health; Medical Devices and Combination Products; Voluntary Malfunction Summary Reporting Program for Manufacturers | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2017-12-26T05:00:00Z | 2017 | 12 | 2017-12-26T05:00:00Z | 2018-02-27T04:59:59Z | 2024-08-29T18:24:28Z | 2017-27650 | 0 | 0 | 0900006482d7293c |
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CREATE TABLE documents (
id TEXT PRIMARY KEY,
agency_id TEXT,
docket_id TEXT REFERENCES dockets(id),
title TEXT,
document_type TEXT,
subtype TEXT,
posted_date TEXT,
posted_year INTEGER,
posted_month INTEGER,
comment_start_date TEXT,
comment_end_date TEXT,
last_modified TEXT,
fr_doc_num TEXT,
open_for_comment INTEGER,
withdrawn INTEGER,
object_id TEXT
);
CREATE INDEX idx_docs_agency ON documents(agency_id);
CREATE INDEX idx_docs_docket ON documents(docket_id);
CREATE INDEX idx_docs_date ON documents(posted_date);
CREATE INDEX idx_docs_year ON documents(posted_year);
CREATE INDEX idx_docs_type ON documents(document_type);
CREATE INDEX idx_docs_frnum ON documents(fr_doc_num);
CREATE INDEX idx_docs_comment_end ON documents(comment_end_date) WHERE comment_end_date IS NOT NULL AND withdrawn = 0;