17 spine devices receive FDA 510(k) clearance in March 2017 Featured

Written by  Laura Dyrda | Wednesday, 19 April 2017 06:42
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The FDA cleared 17 spine-related devices in March.

1. Medicon Spinal Spreading Systems from Medicon EG.


2. NuVasive Next Generation NVM5 System from NuVasive.


3. VertebraLINK Fusion Platform from LINKSPINE.


4. iFuse Implant System – iFuse-3D implant from SI-BONE.


5. GPC Brand Posterior, Non-cervical Pedicle Screw Spinal System from GPC Medical.


6. NuVasive Modulus XLIF Interbody System from NuVasive.


7. Mojave Expandable Interbody System from K2M.


8. Rampart T Lumbar Interbody Fusion Device from Spineology.


9. Cavux CervicalCage-L System from Providence Medical Technology.


10. NuVasive CoRoent Small Interbody System from NuVasive.


11. SeaSpine Daytona Small Stature Spinal System from SeaSpine Orthopedics.


12. NuVasive Reline 4.5-5.0 System from NuVasive.


13. LOSPA IS TLIF & DLIF Cages from Corentec.


14. NuVasive Monolith Corpectomy System form NuVasive.


15. Precice Intramedullary Limb Lengthening System from NuVasive Specialized Orthopedics.


16. Altus Spine Titanium Interbody Fusion System from Altus Partners.


17. Butrex Lumbar Buttress Plating System from X-Spine Systems.


More articles on spine devices:
Implanet revenue up 3% in Q1: 5 things to know
Amendia acquires Spinal Elements
Zimmer Biomet, Medtronic, Stryker & more: 18 device company key notes

Last modified on Thursday, 20 April 2017 14:32
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