FDA 510(k) Applications Submitted by US SPINE

FDA 510(k) Number Submission Date Device Name Applicant
K082801 09/24/2008 PHANTOM PLUS CAGE SYSTEM US SPINE
K061041 04/14/2006 US SPINE FACET FIXATION SYSTEM US SPINE
K081883 07/02/2008 MODIFICATION TO PREFERENCE PEDICLE SCREW SYSTEM US SPINE
K062785 09/18/2006 LTD POLYAXIAL FIXATION SYSTEM US SPINE
K081296 05/07/2008 PREFERENCE PEDICLE SCREW SYSTEM US SPINE


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