Neurological Devices Panel of the Medical Devices Advisory Committee; Notice of Meeting; Correction
The Food and Drug Administration (FDA) is correcting a notice that appeared in the Federal Register of Friday, December 7, 2012 (77 FR 73034). The product name in the document w...
The Food and Drug Administration (FDA) is correcting a notice that appeared in the
Federal Register
of Friday, December 7, 2012 (77 FR 73034). The product name in the document was incorrect. This document corrects that error.
FOR FURTHER INFORMATION CONTACT:
Natasha Facey, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Ave., Silver Spring, MD 20993, 301-796-5290,
Natasha.Facey@fda.hhsgov.
SUPPLEMENTARY INFORMATION:
In FR doc. 2012-29538, appearing on page 73034 in the
Federal Register
of Friday, December 7, 2012, the following correction is made:
1. On page 73034, in the second column under the section entitled “Agenda”, the product name “NeuroPace Responsive Neurostimulation (RNS) System” is corrected to read “NeuroPace RNS System”.
Dated: December 7, 2012.
Jill Hartzler Warner,
Acting Associate Commissioner for Special Medical Programs.
Use this for formal legal and research references to the published document.
77 FR 74197
Web Citation
Suggested Web Citation
Use this when citing the archival web version of the document.
“Neurological Devices Panel of the Medical Devices Advisory Committee; Notice of Meeting; Correction,” thefederalregister.org (December 13, 2012), https://thefederalregister.org/documents/2012-30024/neurological-devices-panel-of-the-medical-devices-advisory-committee-notice-of-meeting-correction.