K7 has received FDA 510(k) clearance for its K7C Cervical Spacer spinal implant for use as an intervertebral body fusion device.
The K7C uses VESTAKEEP PEEK material for durability. It is one of the first PEEK-based spinal fusion medical devices to gain FDA approval, according to the release.
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The K7C uses VESTAKEEP PEEK material for durability. It is one of the first PEEK-based spinal fusion medical devices to gain FDA approval, according to the release.
More Articles on Supply Chain:
Medical Device Companies Use Additive Manufacturing to Cut Implant Costs
Community Regional Medical Center First to Use New Knee Replacement Device
Pioneer Surgical Technology Opens German Plant