Foundation Surgical’s lateral interbody system earns FDA nod: 3 notes

Foundation Surgical earned FDA 510(k) clearance for its Interwedge standalone lateral interbody system.

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Three things to know:

1. The device can be used in conjunction with the company’s LLIF 180 procedure, according to an Oct. 4 news release. The LLIF 180 procedure is a bilateral-fixated standalone-lateral procedure.

2. The Interwedge’s deployable system makes the LLIF 180 procedure possible and is designed to provide ipsilateral and contralateral fixation.

3. The device and procedure help facilitate a lumbar spinal fusion without the need for  supplemental posterior fixation.

At the Becker’s 32nd Annual Meeting: The Business and Operations of ASCs, taking place October 29-31 in Chicago, ASC leaders, surgeons and healthcare executives will explore strategies to drive growth, enhance operational performance, navigate reimbursement challenges and prepare for the future of ambulatory surgery. Apply for complimentary registration now.

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Is ambulatory care healthcare’s big margin engine? 4 leaders weigh in

Wednesday, July 29
1:00 PM - 2:00 PM CDT

Presenters: Joe Ganley, athenahealthJeffrey Flynn, CASC, Gramercy Surgery CenterBryan Tsao, Access Center, Loma Linda University HealthJason Zepeda, Northridge Hospital Medical Center, CommonSpirit HealthGreg DeConciliis, PA-C, CASC, Boston Out­Patient Surgical Suites

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