Nuvectra seeks FDA MRI-conditional approval for Algovita SCS system — 3 notes

Nuvectra filed a regulatory submission with the FDA for full-body MRI-conditional approval for its Algovita SCS system.

Advertisement

Here are three notes:

 

1. The Algovita SCS system is a CE marked and FDA approved for treating trunk and limb chronic pain.

 

2. Nuvectra hopes to have MRI-conditional approval by the end of 2017, following the 180-day review process.

 

3. The Algovita SCS system is Nuvectra’s first commercial offering.

 

More articles on devices:
Jon Stryker is Michigan’s top philanthropist, donating $336M in the state since 2000
Medtronic’s Luann Pendy on diversity in the medical device field: 7 key thoughts
K2M reveals SAHARA AL Expandable Stabilization System: 5 takeaways

Nuvectra seeks FDA MRI-conditional approval for Algovita SCS system — 3 notes (devices, fp)

 

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

Advertisement

Comments are closed.