ACDF system cleared by FDA

Spinal Tech

VySpine's ClariVy cervical IBF system for anterior cervical discectomy with fusion cases was cleared by the FDA.

The device is made from Peek Optima LT1 or Peek Optima HA-enhanced material, according to a Feb. 1 news release. It is designed to create better bony apposition to the implant. The device is offered in multiple footprints and heights and lordosis. 

"The ClariVy Cervical IBF System is the first in a series of differentiated interbody systems being developed by VySpine. … This is just the next step in a series of exciting, innovative product launches scheduled for 2022," CEO Tom McLeer said in the release.

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