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 Date: 2013-10-09 09:33:36Health Synthes Medical device Screw Predicate Center for Devices and Radiological Health Premarket approval Title 21 of the Code of Federal Regulations Medicine Technology Food and Drug Administration |
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(&SYNTHESS 510(k) Summary Page I of 3 Date Prepared | Microsoft PowerPoint - dittoDocID: 1gc7K - View Document |
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| Federal Register / Vol. 80, NoWednesday, May 6, Notices Submit electronic comments on the draft guidance to http:// www.regulations.gov. Submit written comments to the Division of Dockets Management (HFA–DocID: 1aGhA - View Document |
| This document is scheduled to be published in the Federal Register onand available online at http://federalregister.gov/a, and on FDsys.govP DEPARTMENT OF HEALTH AND HUMAN SERVICESDocID: 1akUI - View Document |
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