Bone Anchors - Premarket Notification (510(k)) Submissions: Guidance for Industry and Food and Drug Administration Staff

Name: Bone Anchors - Premarket Notification (510(k)) Submissions: Guidance for Industry and Food and Drug Administration Staff
Creator: Food and Drug Administration
Keywords: 510k,anchors,bone,fda,guidances,industry,notification,pre-market,pre-market-notification,submissions

Information

Type

Guidance

Regulated products

Medical Devices

Topics

Premarket

Published

March 3, 2020

Last updated

March 2, 2020

Description

This document is a guidance for industry and FDA staff on premarket notification submissions for bone anchors.

Organization

Food and Drug Administration (FDA) 🇺🇸

Country / Region

United States

License

Other (Public Domain)

Feedback

Suggest an improvement to this page

1 Main file

Bone Anchors - Premarket Notification (510(k)) Submissions: Guidance for Industry and Food and Drug Administration Staff

Updated on March 2, 2020

pdf (503.4KB)

URL: https://www.fda.gov/media/72235/download
Permalink: https://data.openrid.co/en/datasets/r/a1c67f82-dcae-456c-8c5b-be64015c7c59
MIME Type: application/pdf

Created on: March 3, 2020
Modified on: March 2, 2020

Size: 503.4KB

Bone Anchors - Premarket Notification (510(k)) Submissions: Guidance for Industry and Food and Drug Administration Staff

Information

Type

Regulated products

Topics

Published

Last updated

Description

Tags

Organization

Country / Region

License

Feedback

Actions

Social networks

Embed