[Trial of device that is not approved or cleared by the U.S. FDA]

This trial has been identified as being associated with a clinical device that has not been approved or cleared by the US Food and Drug Administration. Under the terms of US Public Law 110-85, Title VIII, Section 801, the details of this study are not available to the public.

First Received: December 21, 2007 Last Updated: January 7, 2008 History of Changes

Sponsor:	Biomet Biologics, LLC
Information provided by:	Biomet, Inc.
ClinicalTrials.gov Identifier:	NCT00587613

Responsible Party:	Biomet Biologics, Inc. ( Mary Verstynen )
Study ID Numbers:	PRP-001
Study First Received:	December 21, 2007
Last Updated:	January 7, 2008
ClinicalTrials.gov Identifier:	NCT00587613 History of Changes
Health Authority:	United States: Food and Drug Administration; United States: Institutional Review Board

ClinicalTrials.gov processed this record on February 08, 2010