Icotec earns additional FDA nod for Vader system

Icotec’s Vader pedicle system navigated instruments earned FDA 510(k) clearance, the medtech company said July 27.

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The navigation set includes instruments for open and minimally invasive spine surgery, according to a news release. 

“This clearance opens new opportunities for growth and reaffirms our position as the leader in Carbon/PEEK implants and our commitment to keeping a standard surgical technique,” Icotec CEO, Roger Stadler, said in the release.

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