Minimally invasive spine device gets FDA, CE nods

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

Advertisement

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 23rd Annual Spine, Orthopedic and Pain Management-Driven ASC + The Future of Spine Conference, taking place June 11-13 in Chicago, spine surgeons, orthopedic leaders and ASC executives will come together to explore minimally invasive techniques, ASC growth strategies and innovations shaping the future of outpatient spine care. Apply for complimentary registration now.

Advertisement

Next Up in Spinal Tech

  • From new technology acquisitions to regulatory clearances to leadership changes, here are 20 developments and updates from the biggest players…

  • SurGenTec’s ION-C earned FDA 510(k) clearance for ION-C navigation instruments with the ION-C posterior cervical facet fixation implant, according to…

  • VB Spine has made big pushes into the spine medtech space so far in 2026, including global expansions. Six headlines…

Advertisement

Comments are closed.