Home » Life Spine’s ProLift Spinal System Gets FDA’s 510(k) Clearance
Life Spine’s ProLift Spinal System Gets FDA’s 510(k) Clearance
Life Spine has received the FDA’s 510(k) clearance for its ProLift micro expandable spacer system, a spinal device.
The ProLift micro, which features a self-locking design that is adjustable to the individual patient’s pathology and anatomy, is available in a range of sizes.
The device is intended for “micro invasive” procedures such as endoscopic transforaminal lumbar interbody fusions, the Huntley, Ill.-based company said.
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