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FDA 510(k) Applications Submitted by JANET M WEBB
FDA 510(k) Number
Submission Date
Device Name
Applicant
K131061
04/16/2013
RESTORE BUNION CORRECTION SYSTEM
NEXTREMITY SOLUTIONS
K090707
03/17/2009
TALOS INTERVERTEBRAL BODY FUSION DEVICE
MEDITECH ADVISORS, LLC
K051027
04/22/2005
STALIF TT
SURGICRAFT LTD.
K041469
06/02/2004
ANTERIOR COMPACT SYSTEM
X-SPINE SYSTEMS
K041617
06/15/2004
STALIF TT
SURGICRAFT LTD.
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