CDRHNew
Date: August 22, 2012
The following new items were added to the CDRH web pages on August 21, 2012. Previous CDRH New Items can be found on the CDRHNew Page.
- Class I Medical Device Recall: Synthes Hemostatic Bone Putty
- Public Workshop - Post Approval Studies 2012 Workshop: Design, Methodology, and Role in Evidence Appraisal throughout the Total Product Life Cycle, August 30, 2012
- Federal Register: Post-Approval Studies 2012 Workshop: Design, Methodology, and Role in Evidence Appraisal Throughout the Total Product Life Cycle; Public Workshop; Request for Comments
| This email was sent to kostikblog@ukr.net using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 800-439-1420 |  |
