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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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