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Home » Aurora Spine Gets FDA Clearance for Cervical Interbody System
Aurora Spine Gets FDA Clearance for Cervical Interbody System
August 5, 2021
Aurora Spine has received the FDA’s 510(k) clearance for its DEXA-C cervical cages for use in anterior cervical discectomy with fusion procedures.
The Carlsbad, Calif.-based company says the approval is its first for the patented technology, which creates a series of implants with varying densities to match a patient's bone density.
The system, which is intended to promote faster bone growth, is an alternative to “a one-size-fits-all solution,” as it can be matched with patients to provide “the best chance of long-term fixation and bone, the company said.
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