Tag: SAHARA Lateral

Stryker receives FDA clearance for SAHARA® Lateral 3D

Stryker receives FDA clearance for SAHARA® Lateral 3D

Stryker announced recently the U.S. Food and Drug Administration (FDA) 510(k) clearance of its SAHARA Lateral 3D Expandable Interbody System featuring Lamellar 3D Titanium Technology, which will be on display at the Society for Minimally Invasive Spine Surgery (SMISS) Annual Forum in Las Vegas, NV.