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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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