Alphatec Launches IdentiTi Interbody for ALIF
Alphatec commenced commercial release of the IdentiTi Large Window Porous Titanium Interbody Implant for anterior lumbar interbody fusion....
Alphatec commenced commercial release of the IdentiTi Large Window Porous Titanium Interbody Implant for anterior lumbar interbody fusion....
joimax commenced launch of the complete line of EndoLIF® devices for lumbar interbody fusion....
Safe Orthopaedics' SteriSpine pedicle screw kits have been utilized in 23 procedures in Japan since launch in May 2019....
SeaSpine commenced full launch of the Regatta® minimally invasive lateral interbody fusion system....
icotec was granted FDA 510(k) clearance for VADER®one pedicle screws for minimally invasive and open spine procedures....
Benvenue Medical received FDA 510(k) clearance for the Luna® XD MIS expandable interbody device. Controlled launch will proceed at select centers....
SI-BONE's iFuse Implant System®, introduced in 2009, has been used in >40,000 SI joint fusion procedures by more than 1,900 surgeons...
Innovasis was granted FDA 510(k) clearance to market the LxHA Lateral Interbody Fusion Device....
Life Spine received FDA 510(k) clearance to market the PROLIFT® Lateral Expandable Spacer system....
Medicrea was allowed three new U.S. patents relating to the company's proprietary UNiD® Adaptive Spine Intelligence software platform....
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