The FDA gave Huntley, Ill.-based Life Spine 510(k) clearance for its PLATEAU-C Ti Cervical Spacer System.
Here are four things to know:
1. The FDA has cleared 62 of Life Spine's product lines.
2. Using Life Spine's OSSEO-LOC technology, the device offers a surface technology conducive to potential bone growth.
3. PLATEAU-C Ti has more graft windows than its PEEK counterpart, allowing for more visibility in-situ and bone graft containment.
4. The device entered the market on April 3, 2017.
Life Spine Vice President of Marketing Mariusz Knap said in a release, "As one of the fastest-growing, most innovative companies in our space it is important to our surgeons and patients that we continue to advance the cutting edge of technology."
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