AccelSPINE received U.S. Food and Drug Administration clearance on its Picasso II system.
Aurora Spine received 510(k) clearance from the U.S. Food and Drug Administration for its new ZIP MIS system and for additional sizes of the company’s ZIP ULTRA Minimally Invasive Interspinous Fusion System.
BioMedical Enterprises’ Speed Shift Continuous Active Compression System is now available nationally.
Expanding Orthopedics introduced its FLXfit, its 3D expandable intervertebral TLIF cage.
GS Medical USA released the AnyPlus T/PLIF Cage.
Nextremity Solutions launched the Re+Line Bunion Correction System in the United States for bunion correction surgery.
OrthoPediatrics introduced two new products — the Response Spine System and the OrthoPediatrics Anterior Cruciate Ligament Reconstruction System.
More Articles on Devices:
5 Key Results: LDR’s Mobi-C Artificial Disc Replacement vs. ACDF
FDA Clears AccelSPINE’s Next Generation Minimally Invasive Spine System
Global Medical Device Market to Grow at 6.2% Annually Until 2018
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.
