Icotec earns additional FDA nod for Vader system

Spinal Tech

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

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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