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Co-Ligne AG

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K083567 GII SPINAL FIXATION SYSTEM, GII-TI-POLY AXIAL SCREWMNH2009-09-14 View
510(k) K072326 OSTAPEK VBR SYSTEMMQP2008-06-24 View
510(k) K051089 GII SPINAL FIXATION SYSTEMMNH2005-10-26 View
510(k) K032604 GII SPINAL FIXATION SYSTEMMNH2004-01-20 View
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