17 Spine Devices Receives FDA 510(k) Clearance in October

Written by Laura Dyrda | November 05, 2013 | Print  |

InstrumentsThe Food and Drug Administration granted 17 spine-related device clearances in October.

1. Everest Spinal System from K2M.

 

2. Pass LP Spinal System from Medicrea International.

 

3. Nautilus Spinal System from Life Spine.

 

4. MagniFuse Bone Graft, MagiFuse II Bone Graft from Medtronic Sofamor Danek.

 

5. STAXX IBL System from Spine Wave.

 

6. CD Horizon Spinal System from Medtronic Sofamor Danek.

 

7. Anterior Lumbar Plate System (Presidio) from Life Spine.

 

8. Cezanne II Interbody Fusion System from Accel Spine.

 

9. Inertia MIS Pedicle Screw System from Nexxt Spine.

 

10. Idys LIF Cages from Clariance.

 

11. Implanet Spine System from Implanet.

 

12. iFuse Implant System from SI-BONE.

 

13. True Spinal Fixation System from Innovative Surgical Designs.

 

14. Calix Lumbar Spinal Implant System from X-Spine Systems.

 

15. Lotus from Spinal Elements.

 

16. Marauder Cervical-Thoracic Spinal Fixation System from Intelligent Implant Systems.

 

17. Nautilus Spinal System from Life Spine.

 

More Articles on Spine Devices:
18 Spine Devices Receive FDA 510(k) Clearance in September
20 Spine Devices Receive FDA 510(k) Clearance in August
12 Spine Devices Receive FDA 510(k) Clearance in July

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