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Six important government approvals for your practice
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Spine Surgery Today has highlighted six stories of drugs and devices receiving government approval to keep your practice up-to-date.
Spinal Elements announces clearance, upcoming launch of new implants
Spinal Elements recently announced it has received FDA clearance for a full line of interbody devices with Ti-Bond coating for use in the cervical spine. Read more.
Valorem Surgical announces FDA clearance of new spinal fixation system
Valorem Surgical recently announced the receipt of FDA clearance for its minimally invasive MaxiMIS Spinal Fixation System. Read more.
Vexim receives FDA approval for marketing of new cement system
Vexim announced recently that the U.S. Food and Drug Administration has approved the company’s Masterflow Injection System, designed for mixing and injecting orthopedic cement, for marketing within the U.S. Read more.
Titan Spine receives FDA clearance for new surface technology
Titan Spine announced it has received 510(k) clearance from the U.S. Food and Drug Administration to market its Endoskeleton line of interbody fusion implants featuring its nanoLOCK surface technology. Read more.
Benvenue Medical receives FDA clearance for new fusion device
Benvenue Medical announced today that the company’s Luna 360 Interbody Fusion System has received 510(k) clearance from the U.S. Food and Drug Administration for spinal fusion treatment of symptomatic degenerative disc disease. Read more.
Nanovis granted 510(k) clearance for FortiCore interbody fusion devices
Nanovis Spine recently announced it has received U.S. Food and Drug Administration 510(k) clearance for its sterile-packed FortiCore interbody fusion devices. Read more.