ACDF system cleared by FDA

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

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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.

At the Becker’s 32nd Annual Meeting: The Business and Operations of ASCs, taking place October 29-31 in Chicago, ASC leaders, surgeons and healthcare executives will explore strategies to drive growth, enhance operational performance, navigate reimbursement challenges and prepare for the future of ambulatory surgery. Apply for complimentary registration now.

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