Medical Device Manufacturer · US , Apple Valley , MN

Captiva Spine - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2012
7
Total
7
Cleared
0
Denied

Captiva Spine has 7 FDA 510(k) cleared medical devices. Based in Apple Valley, US.

Historical record: 7 cleared submissions from 2012 to 2016. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Captiva Spine Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Captiva Spine
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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