Retrospective Review of Premarket Approval Application Devices; Striking the Balance Between Premarket and Postmarket Data Collection; Correction

---
identifier: "/us/fr/2015-13337"
source: "fr"
legal_status: "authoritative_unofficial"
title: "Retrospective Review of Premarket Approval Application Devices; Striking the Balance Between Premarket and Postmarket Data Collection; Correction"
title_number: 0
title_name: "Federal Register"
section_number: "2015-13337"
section_name: "Retrospective Review of Premarket Approval Application Devices; Striking the Balance Between Premarket and Postmarket Data Collection; Correction"
positive_law: false
currency: "2015-06-02"
last_updated: "2015-06-02"
format_version: "1.1.0"
generator: "[email protected]"
agency: "Health and Human Services Department"
document_number: "2015-13337"
document_type: "notice"
publication_date: "2015-06-02"
agencies:
  - "Health and Human Services Department"
  - "Food and Drug Administration"
fr_citation: "80 FR 31386"
fr_volume: 80
docket_ids:
  - "Docket No. FDA-2015-N-1805"
fr_action: "Notice; request for comments; correction."
---


#  Retrospective Review of Premarket Approval Application Devices; Striking the Balance Between Premarket and Postmarket Data Collection; Correction

**AGENCY:**

Food and Drug Administration, HHS.

**ACTION:**

Notice; request for comments; correction.

**SUMMARY:**

The Food and Drug Administration is correcting a notice entitled “Retrospective Review of Premarket Approval Application Devices; Striking the Balance Between Premarket and Postmarket Data Collection” that appeared in the *Federal Register* of April 29, 2015 (80 FR 23798). The document announced the progress of the Center for Devices and Radiological Health on its 2014-2015 Strategic Priority “Strike the Right Balance Between Premarket and Postmarket Data Collection.” The document was published with the incorrect docket number. This document corrects that error.

**FOR FURTHER INFORMATION CONTACT:**

Lisa Granger, Office of Policy and Planning, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 32, Rm. 3330, Silver Spring, MD 20993-0002, 301-796-9115.

**SUPPLEMENTARY INFORMATION:**

In the *Federal Register* of April 29, 2015, in FR Doc. 2015-09884, on page 23798, the following correction is made:

1. On page 23798, in the first column, in the headings section of the document, “[Docket No. FDA-2014-D-0090]” is corrected to read “[Docket No. FDA-2015-N-1805]”.

Dated: May 28, 2015.

Leslie Kux,

Associate Commissioner for Policy.