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FDA 510(k) Applications Submitted by CO-LIGNE AG
FDA 510(k) Number
Submission Date
Device Name
Applicant
K032604
08/25/2003
GII SPINAL FIXATION SYSTEM
CO-LIGNE AG
K072326
08/20/2007
OSTAPEK VBR SYSTEM
CO-LIGNE AG
K051089
04/28/2005
GII SPINAL FIXATION SYSTEM
CO-LIGNE AG
K083567
12/03/2008
GII SPINAL FIXATION SYSTEM, GII-TI-POLY AXIAL SCREW
CO-LIGNE AG
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