Medical Device Manufacturer · US , Apple Valley , MN

Captiva Spine - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2012

Recent clearances: Captiva Spine and CapLOX II/TowerLOX Pedicle Screw System, CapLOX II/TowerLOX Pedicle Screw System, Captiva Spine SmartLOX Cervical Plate System

View 7 510(k) Devices ↓
7
Total
7
Cleared
0
Denied

FDA 510(k) Regulatory Record - Captiva Spine Orthopedic ✕

7 devices
1-7 of 7
Cleared Mar 02, 2016
Captiva Spine and CapLOX II/TowerLOX Pedicle Screw System
K160020 · MNH
Orthopedic · 57d
Cleared Jun 26, 2015
CapLOX II/TowerLOX Pedicle Screw System
K151116 · MNH
Orthopedic · 60d
Cleared Jun 11, 2015
Captiva Spine SmartLOX Cervical Plate System
K141332 · KWQ
Orthopedic · 386d
Cleared May 28, 2015
Captiva Spine FuselOX Cervical IBF System
K142586 · ODP
Orthopedic · 255d
Cleared Aug 08, 2013
CAPLOX II PEDICLE SCREW SYSTEM/TOWERLOX PEDICLE SCREW SYSTEM
K131538 · MNH
Orthopedic · 71d
Cleared Oct 25, 2012
FUSELOX LUMBAR INTERBODY FUSION DEVICE
K122956 · MAX
Orthopedic · 30d
Cleared Oct 16, 2012
TOWERLOX PEDICLE SCREW SYSTEM
K122332 · MNI
Orthopedic · 75d
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