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

The FDA granted 15 spine-related device clearances in February.

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1. Zyston Strut Open Titanium Spacer System from Zimmer Biomet.

2. Tryptik2 C-Plate Anterior Cervical Plate System from Spineart.

3. The Plateau-LO Spacer System from Life Spine.

4. Cascadia Interbody System from K2M.

5. NuVasive MLX – Medial Lateral Expandable Lumbar Interbody System; NuVasive AP Expandable XLIF System from NuVasive.

6. The Solstice OCT System from Life Spine.

7. Cavetto-SA Cervical Cage System from NeuroStructures.

8. Seurat Universal Pedicle Screw System from CTL Medical Corporation.

9. Alta Anterior Cervical Interbody Spacer from Astura Medical.

10. SeaSpine Spinous Process System from SeaSpine Orthopedics.

11. Endoskeleton TAS Interbody Fusion, Endoskeleton TAS Hyperlordotic Interbody Fusion Device from Titan Spine.

12. Camber Spine Technologies Spira-V Open Matrix Corpectomy Cage from Camber Spine Technologies.

13. SeaSpine Mariner Pedicle Screw System from SeaSpine Orthopedics.

14. UNiD Spine Analyzer from Medicrea International.

15. SeaSpine NewPort Spinal System from SeaSpine Orthopedics.

More articles on spine devices:
10 things to know about Medtronic
K2M launches spinal system: 5 things to know
Alphatec acquires neuromonitoring technology provider for $18M+: 5 things to know

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