22 Spine Devices Receive FDA 510(k) Clearance in February

The Food and Drug Administration granted 22 spine-related 510(k) clearances in February.
1. NuVasive Long Lateral Spinal System from NuVasive.

2. EasySpine System from LDR Spine.

3. Anterior Cervical Plate System from Weigao Orthopaedic Device.

4. Pass LP Spinal System from Medicrea International.

5. Maxim Surgical X-Treme Interbody Fusion System from Maxim Surgical.

6. Reliance Spinal Screw System from Reliance Medical Systems.

7. Xiphos from DiFusion Technologies.

8. Spectrum Spine Laminoplasty Plating Systems from Spectrum Spine.

9. Spineology Spinous Process Plate from Spineology.

10. Espine from NLT Spine.

11. Gibralt Occipital Plate Screws from Exactech.

12. Range Spinal System, Small Stature Components from K2M.

13. Medtronic Strata NSC Lumboperitoneal Valve and Shunt System from Medtronic Neurosurgery.

14. Illico MIS Posterior Fixation System from Alphatec Spine.

15. Synster (Cervical ALIF, PLIF, PTLIF, and TLIF) from BM Korea.

16. Spine Frontier PedFuse Pedicle Screw System from Spine Frontier.

17. Lucent from Spinal Elements.

18. CD Horizon Spinal System from Medtronic Sofamor Danek.

19. Vertex Reconstruction System from Medtronic Sofamor Danek.

20. Polaris Spinal System-Ballista II Percutaneous Screw Placement System from Biomet Spine.

21. SImmetry Sacroiliac Joint Fusion System from Zyga Technology.

22. Intervertebral Body Fusion Device from Dio Medical.

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11 Spine Devices Receive FDA 510(k) Clearance in January
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