[Federal Register Volume 64, Number 221 (Wednesday, November 17, 1999)]
[Notices]
[Pages 62678-62679]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 99-29916]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 99P-4064]
Medical Devices; Exemptions From Premarket Notification; Class II
Devices
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
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SUMMARY: The Food and Drug Administration (FDA) is announcing that it
has received a petition requesting an exemption from the premarket
notification requirements for vascular tunnelers. FDA is publishing
this notice in order to obtain comments on this petition in accordance
with procedures established by the Food and Drug Administration
Modernization Act of 1997 (FDAMA).
DATES: Written comments by December 17, 1999.
ADDRESSES: Submit written comments on this notice to the Dockets
Management Branch (HFA-305), Food and Drug Administration, 5630 Fishers
Lane, rm. 1061, Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT: Heather S. Rosecrans, Center for
Devices and Radiological Health (HFZ-404), Food and Drug
Administration, 9200 Corporate Blvd., Rockville, MD 20850, 301-594-
1190.
SUPPLEMENTARY INFORMATION:
I. Statutory Background
Under section 513 of the Federal Food, Drug, and Cosmetic Act (the
act) (21 U.S.C. 360c), FDA must classify devices into one of three
regulatory classes: Class I, class II, or class III. FDA classification
of a device is determined by the amount of regulation necessary to
provide a reasonable assurance of safety and effectiveness. Under the
Medical Device Amendments of 1976 (the 1976 amendments (Public Law 94-
295)), as amended by the Safe Medical Devices Act of 1990 (Public Law
101-629), devices are to be classified into class I (general controls)
if there is information showing that the general controls of the act
are sufficient to assure safety and effectiveness; into class II
(special controls), if general controls, by themselves, are
insufficient to provide reasonable assurance of safety and
effectiveness, but there is sufficient information to establish special
controls to provide such assurance; and into class III (premarket
approval), if there is insufficient information to support classifying
a device into class I or class II and the device is a life-sustaining
or life-supporting device or is for a use that is of substantial
importance in preventing impairment of human health, or presents a
potential unreasonable risk of illness or injury.
Most generic types of devices that were on the market before the
date of the 1976 amendments (May 28, 1976) (generally referred to as
preamendments devices) have been classified by FDA under the procedures
set forth in section 513(c) and (d) of the act through the issuance of
classification regulations into one of these three regulatory classes.
Devices introduced into interstate commerce for the first time on or
after May 28, 1976 (generally referred to as postamendments devices)
are classified through the premarket notification process under section
510(k) of the act (21 U.S.C. 360(k)). Section 510(k) of the act and the
implementing regulations (21 CFR part 807) require persons who intend
to market a new device to submit a premarket notification report
(510(k)) containing information that allows FDA to determine whether
the new device is ``substantially equivalent'' within the meaning of
section 513(i) of the act to a legally marketed device that does not
require premarket approval.
On November 21, 1997, the President signed into law FDAMA (Public
Law 105-115). Section 206 of FDAMA, in part, added a new section 510(m)
to the act. Section 510(m)(1) of the act requires FDA, within 60 days
after enactment of FDAMA, to publish in the Federal Register a list of
each type of class II device that does not require a report under
section 510(k) of the act to provide reasonable assurance of safety and
effectiveness. Section 510(m) of the act further provides that a 510(k)
will no longer be required for these devices upon the date of
publication of the list in the Federal Register. FDA published that
list in the Federal Register of January 21, 1998 (63 FR 3142). In the
Federal Register of November 3, 1998 (63 FR 59222), FDA published a
final rule codifying those exemptions.
Section 510(m)(2) of the act provides that, 1 day after date of
publication of the list under section 510(m)(1), FDA may exempt a
device on its own initiative or upon petition of an interested person,
if FDA determines that a 510(k) is not necessary to provide reasonable
assurance of the safety and effectiveness of the device. This section
requires FDA to publish in the Federal Register a notice of intent to
exempt a device, or of the petition, and to provide a 30-day comment
period. Within 120 days of publication of this document, FDA must
publish in the Federal Register its final determination regarding the
exemption of the device that was the subject of the notice. If FDA
fails to respond to a petition under this section within 180 days of
receiving it, the petition shall be deemed granted.
II. Criteria for Exemption
There are a number of factors FDA may consider to determine
whether a 510(k) is necessary to provide reasonable assurance of the
safety and effectiveness of a class II device. These factors are
discussed in the guidance the agency issued on February 19, 1998,
entitled ``Procedures for Class II Device Exemptions from Premarket
Notification, Guidance for Industry and CDRH Staff.'' That guidance can
be obtained through the World Wide Web (WWW) on the CDRH home page at
http://www.fda.gov/cdrh or by facsimile through CDRH Facts-on-Demand at
1-800-899-0381 or 301-827-0111. Specify ``159'' when prompted for the
document shelf number.
III. Petitions
On September 14, 1999, FDA received a petition from IMPRA, Inc.,
requesting an exemption from premarket notification for vascular
tunnelers. Vascular tunnelers are currently classified under 21 CFR
870.3460 as an accessory.
IV. Comments
Interested persons may, on or before December 17, 1999, submit to
the
[[Page 62679]]
Dockets Management Branch (address above) written comments regarding
this notice. Two copies of any comments are to be submitted, except
that individuals may submit one copy. Comments are to be identified
with the docket number found in brackets in the heading of this
document. The petitions and received comments may be seen in the office
above between 9 a.m. and 4 p.m., Monday through Friday.
Dated: November 4, 1999.
Linda S. Kahan,
Deputy Director for Regulations Policy, Center for Devices and
Radiological Health.
[FR Doc. 99-29916 Filed 11-16-99; 8:45 am]
BILLING CODE 4160-01-F