Spine Innovation interbody implant earns FDA nod

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Spine Innovation’s Logic titanium implant system earned FDA 510(k) clearance, according to a Jan. 26 news release.

The device is the next generation of the company’s implant system which has been used in the U.S. for 10 years. Logic’s patented design has a reduced profile and more than doubles in size during expansion.

The new generation implant system incorporates OsteoSync Ti, a patented pure titanium lattice material.

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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