FDA Clearance Given to New 3D Printed Devices

Following in the recent footsteps of SI-BONE's iFuse-3D Implant and Cellular Titanium spinal implants by EIT, two more medical device companies have announced this week that they have received the all-important (510)k clearance from the US Food and Drug Administration (FDA) for 3D printed titanium spinal implants. First up is Camber Spine Technologies, located in Pennsylvania and dedicated to exploring the next level of implant design by creating minimally invasive access solutions that are designed by surgeons to treat spinal issues. Headquartered in California, Renovis Surgical Technologies has also received FDA clearance, and will be able to bring its posterior lumbar Tesera porous titanium interbody fusion systems to the US market. Read more at 3DPrint.com: http://3dprint.com/184298/renovis-camber-fda-clearance/

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