21 CFR Part 872 - DENTAL DEVICES | Title 21 - Food and Drugs | Code of Federal Regulations

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Authority:

21 U.S.C. 351, 360, 360c, 360e, 360j, 371.

Source:

52 FR 30097, Aug. 12, 1987, unless otherwise noted.

Editorial Note:

Nomenclature changes to part 872 appear at 73 FR 35341, June 23, 2008.

Title 21 published on 2012-04-01

The following are only the Rules published in the Federal Register after the published date of Title 21.

For a complete list of all Rules, Proposed Rules, and Notices view the Rulemaking tab.

2013-03-26; vol. 78 # 58 - Tuesday, March 26, 2013

78 FR 18233 - Medical Devices; Technical Amendment

GPO FDSys XML | Text

Additional Documents

type	regulations.gov
FR Doc.	2013-06826
RIN
Docket No.	FDA-2013-N-0011

DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration

Final rule; technical amendment.

This rule is effective March 26, 2013.

21 CFR Parts 814, 822, 862, 864, 866, 868, 870, 872, 874, 876, 878, 880, 882, 884, 886, 888, 890, and 892

Summary

The Food and Drug Administration (FDA) is amending certain medical device regulations to correct minor errors in the Code of Federal Regulations (CFR). This action is editorial in nature and is intended to provide accuracy and clarity to the Agency's regulations.

This is a list of United States Code sections, Statutes at Large, Public Laws, and Presidential Documents, which provide rulemaking authority for this CFR Part.

This list is taken from the Parallel Table of Authorities and Rules provided by GPO [Government Printing Office].

It is not guaranteed to be accurate or up-to-date, though we do refresh the database weekly. More limitations on accuracy are described at the GPO site.

United States Code

USC : Title 21 - FOOD AND DRUGS

§ 360c - Classification of devices intended for human use

Title 21 published on 2012-04-01

The following are ALL rules, proposed rules, and notices (chronologically) published in the Federal Register relating to 21 CFR 872 after this date.

2013-03-26; vol. 78 # 58 - Tuesday, March 26, 2013

78 FR 18233 - Medical Devices; Technical Amendment

GPO FDSys XML | Text

Additional Documents

type	regulations.gov
FR Doc.	2013-06826
RIN
Docket No.	FDA-2013-N-0011

DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration

Final rule; technical amendment.

This rule is effective March 26, 2013.

21 CFR Parts 814, 822, 862, 864, 866, 868, 870, 872, 874, 876, 878, 880, 882, 884, 886, 888, 890, and 892

Summary

The Food and Drug Administration (FDA) is amending certain medical device regulations to correct minor errors in the Code of Federal Regulations (CFR). This action is editorial in nature and is intended to provide accuracy and clarity to the Agency's regulations.

2013-02-07; vol. 78 # 26 - Thursday, February 7, 2013

78 FR 9010 - Dental Devices; Reclassification of Temporary Mandibular Condyle Prosthesis

GPO FDSys XML | Text

Additional Documents

type	regulations.gov
FR Doc.	2013-02688
RIN
Docket No.	FDA-2012-N-1239

DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration

Proposed order.

Submit either electronic or written comments on this proposed order or on the draft guideline by May 8, 2013. See section XIII of this document for the proposed effective date of any final order that may publish based on this proposed order.

21 CFR Part 872

Summary

The Food and Drug Administration (FDA) is issuing a proposed order to reclassify temporary mandibular condyle prosthesis, a preamendments class III device, into class II (special controls), and rename the device “temporary mandibular condyle reconstruction plate.” FDA is also issuing the draft special controls guideline, “Class II Special Controls Guideline: Temporary Mandibular Condyle Reconstruction Plate,” which sets forth the special controls that the Agency believes are necessary to provide a reasonable assurance of the safety and effectiveness of the device.

2013-01-14; vol. 78 # 9 - Monday, January 14, 2013

78 FR 2647 - Dental Devices; Reclassification of Blade-Form Endosseous Dental Implant

GPO FDSys XML | Text

Additional Documents

type	regulations.gov
FR Doc.	2013-00388
RIN
Docket No.	FDA-2012-N-0677

DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration

Proposed order.

Submit either electronic or written comments on this proposed order by April 15, 2013. See section XI of this document for the proposed effective date of a final order based on this proposed order.

21 CFR Part 872

Summary

The Food and Drug Administration (FDA) is proposing to reclassify the blade- form endosseous dental implant, a preamendments class III device, into class II (special controls). On its own initiative, based on new information, FDA is proposing to revise the classification of blade-form endosseous dental implants.

21 CFR Part 872 - DENTAL DEVICES

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