Medical Devices; Pediatric Uses of Devices; Requirements for Submission of Information, etc.:

Federal Register: July 20, 2010 (Volume 75, Number 138)

Rules and Regulations

Page 41986

From the Federal Register Online via GPO Access [wais.access.gpo.gov]

DOCID:fr20jy10-7

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration 21 CFR Part 814

Docket No. FDA-2009-N-0458

RIN 0910-AG29

Medical Devices; Pediatric Uses of Devices; Requirements for

Submission of Information on Pediatric Subpopulations That Suffer From a Disease or Condition That a Device Is Intended to Treat, Diagnose, or

Cure; Withdrawal

AGENCY: Food and Drug Administration, HHS.

ACTION: Direct final rule; withdrawal.

SUMMARY: The Food and Drug Administration (FDA) published in the

Federal Register of April 1, 2010, a direct final rule that was intended to make noncontroversial amendments to existing regulations which would require the submission of readily available pediatric medical device information as a part of premarket approval applications, requests for humanitarian use device exemptions, and any product development protocols. The comment period closed on June 15, 2010. FDA is withdrawing the direct final rule because the agency received significant adverse comment.

DATES: The direct final rule published at 75 FR 16347, April 1, 2010, is withdrawn on July 19, 2010.

FOR FURTHER INFORMATION CONTACT: Robert Gatling, Center for Devices and

Radiological Health, Food and Drug Administration, 10903 New Hampshire

Ave., Bldg. 66, rm. 1640, Silver Spring, MD 20993, 301-796-6560.

Therefore, under the Federal Food, Drug, and Cosmetic Act, and under authority delegated to the Commissioner of Food and Drugs, the direct final rule published on April 1, 2010, at 75 FR 16347 is withdrawn.

Dated: July 9, 2010.

Leslie Kux,

Acting Assistant Commissioner for Policy.

FR Doc. 2010-17617 Filed 7-19-10; 8:45 am

BILLING CODE 4160-01-S