Orthofix Gains FDA Clearance for FORZA XP Expandable Spacer
Orthofix received FDA 510(k) clearance to market the FORZA® XP Expandable Spacer for posterior and transforaminal lumbar interbody fusion....
Orthofix received FDA 510(k) clearance to market the FORZA® XP Expandable Spacer for posterior and transforaminal lumbar interbody fusion....
SeaSpine expanded the Ventura NanoMetalene® interbody line to include sizes that accommodate a larger range of posterior procedures and more...
Two-year study results indicate that decompression plus use of Paradigm Spine's coflex® Interlaminar Stabilization® device may enhance the procedure's durability and...
Spine Wave launched the GraftMag® bone graft delivery system for thoracolumbar spinal fusion procedures....
Kleiner Device Labs introduced KG® 1, a disposable single-use bone graft delivery tool for spinal procedures....
First study cases are complete in Spineology's postmarket investigation of the Duo Lumbar Interbody Fusion system....
NuVasive launched COALESCE for Thoracolumbar Interbody Fusion, and announced FDA 510(k) clearance to market the COHERE® Cervical Interbody Fusion device with expanded indications....
Initial outcomes from Zyga's EVSI study indicate a significant reduction in low back pain and opioid use in patients receiving...
Initial cases are complete and multiple surgeries performed with Life Spine’s SIMPACT™ Tri-Fin Sacroiliac Joint Fusion device, following its November 2017...
FH Orthopedics marked the sale of >6,000 units of its cervical and lumbar artificial discs, CP-ESP® and LP-ESP®....
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