SpineEX® Announces FDA Clearance of Sagittae® Lateral Lumbar Interbody Fusion Devices
FREMONT, Calif., Oct. 10, 2018 /PRNewswire/ -- SpineEX, Inc., a medical device company that aims to provide innovative and minimally invasive implants, high-value disposables and instrumentation for spinal fusion surgeries, announced today it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its Sagittae lateral lumbar interbody fusion (LLIF) device. The LLIF procedure