15 spine devices receive FDA 510(k) clearance in January

Written by Laura Dyrda | February 10, 2020 | Print  |

The FDA cleared 15 spine related devices in January.

1. Nex-D2 Posterior Fixation System from OrthoSurgical.
2. Genesys Spine 3DP Cervical Interbody System from Genesys Spine.
3. Endoskeleton TL Interbody Fusion Device from Titan Spine.
4. Symphony OCT System from Medos International.
5. Evol ha – D Lateral Interbody Fusion System from Cutting Edge Spine.
6. Anatomic PEEK Cervical Fusion System from Medtronic Sofamor Danek.
7. TrellOss-L MPF from Nexxt Spine.
8. Streamline TL Spinal Fixation System from Pioneer Surgical Technology.
9. CD Horizon Fenestrated Screw Set from Medtronic Sofamor Danek.
10. ProLift Expandable System from Life Spine.
11. CapLOX II / TowerLOX MIS Pedicle Screw System from Captiva.
12. SureMAX Family of Cervical Spacers from Additive Implants.
13. M.U.S.T. Pedicle Screw System from Medacta International.
14. Nexxt Matrixx System from Nexxt Spine.
15. CorticaLINK Spinal Fusion Platform from Spine Smith Holdings.

More articles on orthopedic devices:
10 device company executive moves
Maruho Medical acquires orthopedic device company
Atlas Spine launches cervical plating system

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