Neurological Devices Panel of the Medical Devices Advisory Committee; Notice of Meeting; Correction

---
identifier: "/us/fr/2012-30024"
source: "fr"
legal_status: "authoritative_unofficial"
title: "Neurological Devices Panel of the Medical Devices Advisory Committee; Notice of Meeting; Correction"
title_number: 0
title_name: "Federal Register"
section_number: "2012-30024"
section_name: "Neurological Devices Panel of the Medical Devices Advisory Committee; Notice of Meeting; Correction"
positive_law: false
currency: "2012-12-13"
last_updated: "2012-12-13"
format_version: "1.1.0"
generator: "[email protected]"
agency: "DEPARTMENT OF HEALTH AND HUMAN SERVICES"
document_number: "2012-30024"
document_type: "notice"
publication_date: "2012-12-13"
agencies:
  - "DEPARTMENT OF HEALTH AND HUMAN SERVICES"
  - "Food and Drug Administration"
---


#  Neurological Devices Panel of the Medical Devices Advisory Committee; Notice of Meeting; Correction

**AGENCY:**

Food and Drug Administration, HHS.

**ACTION:**

Notice; correction.

**SUMMARY:**

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, *[email protected].*

**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.