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Home » FDA clears LifeSpine anterior lumbar spacer system

FDA clears LifeSpine anterior lumbar spacer system

August 5, 2020 By Sean Whooley

Spinal disorder treatment developer Life Spine announced that it received FDA clearance for its Plateau-A Ti anterior lumbar spacer system.

Huntley, Ill.-based Life Spine’s Plateau-A Ti system can be used for anterior fusion procedures, offering multiple footprint sizes in various heights to accommodate individual anatomies and pathologies, according to a news release.

The system also features large, open graft windows for maximum visibility and bone graft containment, Life Spine’s Osseo-Loc surface treatment technology and a chamfered leading edge to ease implant insertion.

“With the increased usage of anterior column reconstruction, Pleateau-A Ti fills an important portfolio gap,” Life Spine COO Rich Mueller said in the release. “Joining our recently launched Dyna-Link titanium stand-alone ALIF spacer system and Sentry ALIF plating system, this clearance expands our robust ALIF portfolio.

“Continuing our success with previous interbody technologies, Plateau-A Ti provides surgeons with a titanium implant available in a variety of heights, widths, and lordotic options.”

Filed Under: Food & Drug Administration (FDA), Implants, Orthopedics, Regulatory/Compliance, Spine Tagged With: FDA, Life Spine

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About Sean Whooley

Sean Whooley is an associate editor who mainly produces work for MassDevice, Medical Design & Outsourcing and Drug Delivery Business News. He received a bachelor's degree in multiplatform journalism from the University of Maryland, College Park. You can connect with him on LinkedIn or email him at [email protected].

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