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Docket ID: [Docket N0. 2003D-0568]

NOTICE: NOTICES

ACTION: Reports and guidance documents; availability, etc.:

DOCUMENT ACTION: Notice.

SUBJECT CATEGORY: Guidance for Industry and FDA Staff; Class II Special Controls Guidance Document: Vascular and Neurovascular Embolization Devices; Availability

DATES: Submit written or electronic comments on agency guidances at any time.

DOCUMENT SUMMARY: The Food and Drug Administration (FDA) is announcing the availability of the guidance document entitled ``Class II Special Controls Guidance Document: Vascular and Neurovascular Embolization Devices.'' Elsewhere in this issue of the Federal Register, FDA is publishing a final rule to change the names, revise the
identifications, and reclassify the two devices from class III (premarket approval) into class II (special controls). This guidance document describes a means by which the vascular embolization device and the neurovascular embolization device may comply with the requirement of special controls for class II devices. We are also announcing the withdrawal of the 1994 draft guidance document entitled ``Guidance on Biocompatibility Requirements for Long Term Neurological Implants: Part 3Implant Model,'' dated September 12, 1994.

SUMMARY: Medical devices—; Vascular and neurovascular embolization devices; Class II special controls,

SUPPLEMENTAL INFORMATION

In the Federal Register of February 25, 2004 (69 FR 8667), FDA published a proposed rule to reclassify two embolization devices from class III (premarket approval) into class II (special controls). The agency is also changing the names and revising the identifications of these devices. The vascular embolization device (previously the arterial embolization device) is intended to control hemorrhaging due to aneurysms, certain types of tumors, and arteriovenous malformations. The neurovascular embolization device (previously the artificial embolization device) is intended to permanently occlude blood flow to cerebral aneurysms and cerebral arteriovenous malformations.

FDA revised a November 1, 2002, guidance document entitled ``Guidance for Neurological Embolization Devices'' and published it in the Federal Register of February 25, 2004 (69 FR 9667) as a draft class II special controls guidance document to support the reclassification of these device types. Interested persons were invited to comment on the draft guidance by May 25, 2004. FDA received one comment. The comment was supportive of the guidance document but made some suggestions on the guidance's content. FDA considered the suggestions and made appropriate revisions. FDA is now identifying the guidance document entitled ``Class II Special Controls Guidance Document: Vascular and Neurovascular Embolization Devices'' as the guidance document that will serve as the special control for these devices.

The guidance document provides a means by which a vascular embolization device or a neurovascular embolization device may comply with the requirement of special controls for class II devices. Following the effective date of the final reclassification rule, any firm submitting a premarket notification (510(k)) for a vascular embolization device or a neurovascular embolization device will need to address the issues covered in the special controls guidance document. However, the firm need only show that its device meets the recommendations of the guidance document or in some other way provides equivalent assurances of safety and effectiveness.

We are also withdrawing the draft guidance document entitled ``Guidance on Biocompatibility Requirements for Long Term Neurological Implants: Part 3Implant Model'' because it contains outdated information. Archived copies of CDRH guidance documents that have been withdrawn are available from the DSMICA (see ADDRESSES).

II. Significance of Guidance

This guidance is being issued consistent with FDA's good guidance practices regulation (21 CFR 10.115). The guidance represents the agency's current thinking on vascular and neurovascular embolization devices. It does not create or confer any rights for or on any person and does not operate to bind FDA or the public. An alternative approach may be used if the approach satisfies the requirements of the applicable statute and regulations.

III. Electronic Access

To receive a copy of the guidance entitled ``Class II Special Controls Guidance Document: Vascular and Neurovascular Embolization Devices'' by fax machine, call the CDRH FactsOnDemand system at 800 8990381 or 3018270111 from a touchtone telephone. Press 1 to enter the system. At the second voice prompt press 1 to order a document. Enter the document number (1234) followed by the pound sign (). Follow the remaining voice prompts to complete your request.

Persons interested in obtaining a copy of the guidance also may do so by using the Internet. CDRH maintains an entry on the Internet for easy access to information including text, graphics, and files that may be downloaded to a personal computer with Internet access. Updated on a regular basis, the CDRH home page includes device safety alerts, Federal Register reprints, information on premarket submissions (including lists of approved applications and manufacturers' addresses), small manufacturer's assistance, information on video conferencing and electronic submissions, Mammography Matters, and other deviceoriented information. The CDRH Web site may be accessed at http://www/fda/gov/cdrh/guidance.html. IV. Paperwork Reduction Act of 1995

This guidance contains information collection provisions that are subject to review by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995 (44 U.S.C. 35013520) (the PRA). The collections of information addressed in the guidance document have been approved by OMB in accordance with the PRA under the regulations governing 510(k) submissions (21 CFR part 807, subpart E, OMB control number 09100120) and the regulations governing good manufacturing practices (quality system regulation) (21 CFR part 820, OMB control number 09100073). The labeling provisions addressed in the guidance document have been approved by OMB under the PRA, OMB control number 09100485.

V. Comments

Interested persons may submit to the Division of Dockets Management (see ADDRESSES), written or electronic comments regarding this document. Submit a single copy of electronic comments or two paper copies of any mailed comments, except that individuals may submit one paper copy. Comments are to be identified with the docket number found in brackets in the heading of this document. Comments received may be seen in the Division of Dockets Management between 9 a.m. and 4 p.m., Monday through Friday.

Dated: December 15, 2004.
Linda S. Kahan,
Deputy Director, Center for Devices and Radiological Health. [FR Doc. 0428438 Filed 122804; 8:45 am]
BILLING CODE 416001S

FOR FURTHER INFORMATION CONTACT Peter L. Hudson, Center for Devices and Radiological Health (HFZ410), Food and Drug Administration, 9200 Corporate Blvd., Rockville, MD 20850, 3015943090.