VySpine’s LumiVy Lumbar IBF System Cleared

March 10, 2022

VySpine has received the FDA’s 510(k) clearance for its LumiVy lumbar interbody fusion (IBF) system for use after lumbar discectomy surgeries.

Made of polyetheretherketone (PEEK), the implants have an elasticity like that of natural bone and they are radiolucent, meaning that they allow x-ray beams to pass through them.

The implants are available in a variety of sizes and lordosis angles to adjust for the inward curve of the lower spine. The system also features self-drilling screws to aid in anchoring the device directly to bone.

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