FDA 510(k) Applications Submitted by CAPTIVA SPINE

FDA 510(k) Number Submission Date Device Name Applicant
K131538 05/29/2013 CAPLOX II PEDICLE SCREW SYSTEM/TOWERLOX PEDICLE SCREW SYSTEM CAPTIVA SPINE
K122332 08/02/2012 TOWERLOX PEDICLE SCREW SYSTEM CAPTIVA SPINE
K122956 09/25/2012 FUSELOX LUMBAR INTERBODY FUSION DEVICE CAPTIVA SPINE
K151116 04/27/2015 CapLOX II/TowerLOX Pedicle Screw System CAPTIVA SPINE
K141332 05/21/2014 Captiva Spine SmartLOX Cervical Plate System CAPTIVA SPINE
K142586 09/15/2014 Captiva Spine FuselOX Cervical IBF System CAPTIVA SPINE
K160020 01/05/2016 Captiva Spine and CapLOX II/TowerLOX Pedicle Screw System Captiva Spine


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