Tenon Medical’s SImmetry+ sacroiliac joint fusion system earned the FDA’s 510(k) clearance, according to an Oct. 21 news release.
The SImmetry+ system is a minimally invasive lateral access system made of 3D-printed titanium and uses the company’s proprietary instrumentation. Tenon Medical is preparing for an alpha launch aimed for the end of 2025.
SImmetry+ joins the Catamaran SI joint fusion system, which also includes Mainsail and EVoluSIon.
“The introduction of the SImmetry+ SI joint system and its new 3D-printed titanium implant represents a meaningful advancement in SI joint fusion,” Ali Araghi,DO, said in the release. “The porous structure promotes bone ingrowth and biological fixation, while the precision-engineered threads and surface texture enhance initial stability across the joint. Combining these features with the SImmetry system’s simple and proven minimally invasive approach to true arthrodesis has the potential to deliver more consistent fusion outcomes for my patients.”
