Life Spine Announces FDA Clearance of DYNA-LINK Spinal System and PRESIDIO Spinal Plating System

Hoffman Estates, Ill.-based Life Spine has announced that the U.S. Food and Drug Administration has given 510(k) marketing clearance to both the DYNA-LINK Spinal System and the PRESIDIO Spinal Plating System, according to a Life Spine news release.

Advertisement

The DYNA-LINK system features a next-generation stand-alone device that accommodates both fixed and variable angle screws. The PRESIDIO system is a thoracolumbar plating system that features multiple types of low-profile implants. Both offerings incorporate an innovative, zero-step locking mechanism and utilize comprehensive instrumentation designed to reduce surgical steps and intra-operative complexity, according to the release.

“These two approvals are a testament to our commitment to rapidly achieving regulatory approval while at the same time introducing best-in-class products. Furthermore, these products will allow us to realize significant gains in the thoracolumbar fusion space,” Michael S. Butler, Life Spine’s president and CEO, said in the release.

Read the release on the Life Spine FDA clearances.

Advertisement

Next Up in Uncategorized

Advertisement

Comments are closed.