16 spine devices receive FDA 510(k) clearance in July

Written by Laura Dyrda | August 23, 2019 | Print  |

The FDA granted 16 spine-related device clearances last month.

1. UNiD Patient-matched PLIF cage from Medicrea International.

2. Velofix TLIF Cage from U&I Corporation.

3. Tritanium X TL Expandable Lumbar Cage from Stryker Spine.

4. Addivation Medical Cervical Interbody System from Addivation Medical.

5. 4CIS Chiron Spinal Fixation System from Solco Biomedical.

6. ProLift Expandable System from Life Spine.

7. Fortilink IBF System with Tetrafuse 3D Technology from Pioneer Surgical Technology.

8. Favo S-TLIF from Silony Medical.

9. Article-L 3D Ti Spinal System with TiONIC Technology from Medtronic Sofamor Danek.

10. Salvo Spine System from Spine Wave.

11. ExcelsiusGPS Spine 1.1 Interbody Module from Globus Medical.

12. NuVasive Camber Laminoplasty System from NuVasive.

13. Harrier-SA Lumbar Interbody System from ChoiceSpine.

14. Nexxt Matrixx System from Nexxt Spine.

15. Mariner MIS Pedicle Screw System; SeaSpine Navigation System from SeaSpine Orthopedics Corp.

16. Europa Pedicle Screw System from MiRus.

More articles on spine devices:
Aurora Spine posts $3.2M in Q2 revenue: 6 things to know
Medtronic spine revenue up nearly 1% to $658M; robotics grows while spinal cord stimulation slows: 5 details
31 orthopedic devices receive FDA 510(k) clearance in July

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