Please provide your email address to receive an email when new articles are posted on . Sail Fusion announced FDA clearance of its BowTie sacroiliac fusion system. The BowTie system utilizes a ...
DEL MAR, Calif.--(BUSINESS WIRE)--SAIL Fusion, a medical device company focused on advancing the surgical treatment of sacroiliac joint dysfunction through solutions built upon AO principles, today ...
1. Tenon Medical earned FDA 510(k) clearance to use its Catamaran sacroiliac joint system for augmenting thoracolumbar fusion. The indication was first used in June by Andrew Trontis, MD. 2. A new ...
Pain physicians treat the signal, surgeons treat the structure, and insurers evaluate the cost. Patients experience all three. The Elephant in the Room There is an old parable about several blind men ...
Zyga Technology reported the first patient enrollment in Sacroiliac Fusion Study, a prospective, single-arm post-market study designed to evaluate fusion and pain reduction following use of the ...
DEL MAR, Calif.--(BUSINESS WIRE)--SAIL Fusion, a medical device company focused on advancing the surgical treatment of sacroiliac joint dysfunction through solutions built upon proven AO principles, ...
Nevro1™ Proven to Immediately Transfix Sacroiliac (SI) Joint to Allow for Long-term SI Joint Fusion REDWOOD CITY, Calif., Feb. 28, 2024 /PRNewswire/ -- Nevro Corp. (NVRO), a global medical device ...
Genesys Spine Announces Positive Prospective Study Results for SIros® Lateral SI Joint Fusion System
AUSTIN, Texas, Feb. 6, 2026 /PRNewswire/ -- Genesys Spine today announced the results of a prospective multicenter clinical study evaluating the safety and effectiveness of the SIros® Lateral ...
~Clearance expands Company's competitive advantage of clinically proven, minimally invasive technologies to treat debilitating SI joint conditions from multiple surgical approaches~ ~SImmetry+'s New ...
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