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20 spine devices receive FDA 510(k) clearances in July Featured

Written by  Laura Dyrda | Wednesday, 23 August 2017 10:08
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The FDA granted 20 spine device clearances in July.

 

1. Spider Cervical Plating System from X-Spine Systems.

 

2. Spinal Manometer NRFit, Spinal Manometer LUER from PAJUNK GmbH.

 

3. NeoFuse Ti3D PLIF/TLIF/Cervical Interbody from HT Medical.

 

4. Endoskeleton TO Interbody Fusion Device from Titan Spine.

 

5. EIT Cellular Titanium Cervical Cage, PLIF Cages, TLIF, Cages, Alif Cages from EIT Emerging Implant Technologies.

 

6. Coveris Cervical Cage System from Camber Spine Technologies.

 

7. HD Lumbar Interbody System from HD LifeSciences.

 

8. Gemini-C Hybrid Cervical Interbody System from Osseus Fusion Systems.

 

9. Crescent Spinal System from Medtronic Sofamor Danek.

 

10. SeaSpine Cambria System from SeaSpine Orthopedics.

 

11. True Spinal Fixation System from Innovative Surgical Designs.

 

12. Haven Laminoplasty System, Canopy Laminoplasty Fixation System from Globus Medical.

 

13. Eagle Plus Anterior Cervical Plate System from Medos International.

 

14. True Spinal Fixation System from Innovative Surgical Designs.

 

15. Genesys Spine Apache Interbody Fusion System from Genesys.

 

16. Rampart L Lumbar Interbody Fusion Device from Spineology.

 

17. Velofix Interbody Fusion System from U&I Corp.

 

18. OpenLoc-L Spinal Fixation System from L&K Biomed.

 

19. TiLock2 Spinal System from Genesys Spine.

 

20. Vitality Spinal Fixation System from Zimmer Biomet Spine.

 

More articles on spine device clearances:

33 orthopedic devices receive FDA 510(k) clearance in July
48 orthopedic devices receive FDA 510(k) clearance in June
48 orthopedic devices receive FDA 510(k) clearance in May

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