Life Spine Receives Ten 510(k) Clearances in One Year

HUNTLEY, Ill.–(BUSINESS WIRE)–Life Spine, a medical device company that designs, develops,
manufactures and markets products for the surgical treatment of spinal
disorders, announced today that the company received ten 510(k)
clearances in 2018 for a total of 81 since their inception in 2004. The
510(k)’s Life Spine received in 2018 cover a wide variety of procedures
and pathologies.

“We pride ourselves on the ability to rapidly develop new and innovative
technologies that have the potential to improve patient care and quality
of life. This year, receiving ten 510(k) clearances will help us to
maintain our position as an innovation powerhouse,” said Mariusz Knap,
Vice President of Marketing and Business Development for Life Spine.

One key 510(k) clearance that Life Spine secured in 2018 was for the
SIMPACT® Sacroiliac Joint Fixation System. SIMPACT is a novel
sacroiliac screw that was designed to reduce procedural time, decrease
trauma to the surrounding muscles and lessen recovery time by utilizing
a minimally invasive approach. SIMPACT® features Life Spine’s
proprietary OSSEO-LOC® surface technology and a self-drilling
and self-tapping design.

Another notable clearance for Life Spine in 2018 was the PLATEAU®-LO
Spacer System which is a PEEK interbody designed with an oblique
lordosis to better suit patient anatomy. The system’s “Insert and
Rotate” design allows for restoration of disc height and sagittal
alignment, even in severely collapsed disc spaces.

About Life Spine

Life Spine is dedicated to improving the quality of life for spinal
patients by increasing procedural efficiency and efficacy through
innovative design, uncompromising quality standards, and the most
technologically advanced manufacturing platforms. Life Spine, which is
privately held, is based in Huntley, Illinois. For more information,
please visit:

Life Spine is a registered trademark.