Spectrum Spine’s lumbar cages earn FDA clearance

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Spectrum Spine earned FDA 510(k) clearance for its family of lumbar cage implants, according to a July 22 news release.

The implants use BioBraille surface treatment on the bone contact areas and inside the graft window. They’re designed for spinal fusions including ALIF, TLIF, and DLIF.

Spectrum Spine now has 11 spine systems cleared by the FDA.

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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