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

The FDA granted 510(k) clearance to 13 spine devices last month.

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1. Atlas Spine Expandable Cervical Standalone Interbody System from Atlas Spine.
2. Yukon OCT Spinal System from Stryker.
3. Mojave Expandable Interbody System from Stryker.
4. Daytona Small Stature Growth Rod Conversion Set from SeaSpine Orthopedics.
5. Largo PEEK Interbody System from FloSpine.
6. KMTI Teresa SA Anterior Lumbar Interbody Fusion System form Kyocera.
7. Perla TL Posterior Osteosynthesis System from Spineart.
8. Nexxt Matrixx System from Nexxt Spine.
9. OrthoCircle Spine Pedicle Screw System from OrthoCircle Spine.
10. NuVasive X-Core Expandable VBR System from NuVasive.
11. Steerable Plateau Ti from Life Spine.
12. SpineNet SSP System from SpineNet.
13. Daytona Small Stature Spinal System from SeaSpine Orthopedics.

More articles on devices:
5 orthopedic expansion projects costing $200M+
5 recent telemedicine developments for spine, orthopedics
Dr. Scott Boden: Telemedicine can achieve spine success if ‘reimbursement barriers are reduced’

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