Minimally invasive spine device gets FDA, CE nods

Spinal Stabilization Technologies reached two milestones for its PerQdisc spine device.

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The Ireland-based company received the FDA’s “breakthrough designation” and CE mark from the European Union, according to a May 25 news release. PerQdisc is the world’s only commercially available lumbar nucleus replacement system.

The PerQdisc procedure is minimally invasive compared to a spinal fusion or total disc replacement. The device replaces the nucleus pulposus of the intervertebral disc in lower spine in patients with single-level discogenic pain.

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.

Register to Attend Webinar

Is ambulatory care healthcare’s big margin engine? 5 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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