Cervical Spacer System Cleared for Life Spine
Walter Eisner • Mon, May 1st, 2017
The U.S. Food and Drug Administration (FDA) has given 510(k) market clearance to Life Spine, Inc.'s PLATEAU-C Ti Cervical Spacer System.
An April 19, 20917 company announcement states the system offers the company's proprietary titanium surface technology, OSSEO-LOC, which is a surface technology that helps create an environment for potential bone growth. Additionally, in comparison to its PEEK counter-part, PLATEAU-C Ti offers additional graft windows for increased visibility in-situ and bone graft containment.
PLATEAU-C Ti entered a full market release on April 3, 2017.
According to the company's website, the cervical spacers are designed with large, open graft areas for maximum bone graft capacity. The spacers are available in parallel and lordotic versions to accommodate varying patient anatomies.
The company launched 29 products in 2016 and revenues for the year beat the previous year by 38%. It also received six 510(k) clearances for a total of 61 since inception.
Product launches in 2016 included the LONGBOW® Lateral Expandable A/P Spacer System and the PROLIFT® PLIF/TILF Expandable Spacer System.
LONGBOW is the first-to-market product that offers controlled in-situ expansion for maximum endplate coverage, minimal anatomical disruption, and post packing capabilities. Additionally, LONGBOW was selected by Orthopedics This Week for a Spine Technology Award.
PROLIFT features an all titanium implant that restores disc height, in situ, for minimally invasive PLIF and TLIF. Furthermore, the implant is provided pre-sterile for safety and convenience. The company claims to have the broadest, fastest growing suite of expandable products in the market.