NON-SCREW Based Expandable Technology Surgeons and Patients Can Count On

PRESS RELEASE: Expanding Innovations, Inc. (EI) announced today that the company has received 510(k) clearance from the FDA for the X-PAC Expandable Lateral Cage System (X-PAC LLIF).

Expanding Innovations, Inc. (EI), a spinal implant company that designs NON-SCREW based expandable cage technology, announced today that the company has received 510(k) clearance from the FDA for the X-PAC Expandable Lateral Cage System (X-PAC LLIF). This approval marks a significant addition to the company’s expandable product portfolio which also includes the company’s flagship X-PAC Expandable Posterior Cage System (X-PAC TLIF).

Dr. K. Brandon Strenge, Orthopaedic Institute of Western Kentucky, said, “The X-PAC Expandable Lateral Cage System is the first implant I have seen that addresses the core principals of lateral lumbar interbody fusion. The maximized posterior expansion facilitates indirect decompression, the open architecture ensures a bridging bone fusion, and the multiple lordotic options allow proper implant selection for restoration of sagittal balance. These benefits, coupled with the ability to insert the cage at a nominal height, then dial it up via controlled expansion, make X-PAC Lateral an exciting and beneficial technology to offer my patients moving forward.”

Expanding Innovations, Inc. (EI) will feature the new X-PAC Expandable Lateral and X-PAC Expandable Posterior Cage Systems at these upcoming 2023 events:

AAOS Annual Meeting- March 7-11th, visit booth #4259
Spine Summit Annual Meeting- March 16-18th, visit booth #229

For the full press release, visit: https://www.prnewswire.com/news-releases/expanding-innovations-inc-announces-fda-approval-of-x-pac-expandable-lateral-cage-system-301751455.html