FDA 510(k) Applications Submitted by TIM B LUSBY

FDA 510(k) Number Submission Date Device Name Applicant
K100265 01/29/2010 DIAMOND ANTERIOR CERVICAL PLATE SYSTEM AMENDIA, INC.
K050377 02/15/2005 NBD HEAD SCREW NEW BUSINESS DEVELOPMENT, LLC
K961695 05/01/1996 ENDO-TECH LTD., TIPS RATIO DESIGN LAB
K021788 05/31/2002 NBD CEMENT RESTRICTOR DEVICE NEW BUSINESS DEVELOPMENT, LLC
K072029 07/24/2007 PHENIX VERTEBRAL BODY REPLACEMENT NEW BUSINESS DEVELOPMENT, LLC
K032196 07/18/2003 NBD DISPOSABLE RF CANNULAE NEW BUSINESS DEVELOPMENT, LLC


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