Renovis Surgical Receives FDA Clearance for Tesera X Lateral Interbody Fusion System
Renovis Surgical received FDA 510(k) clearance to market the Tesera® X Lateral Interbody Fusion system....
Sep 27, 2018,
Renovis Surgical Receives FDA Clearance for Tesera X Lateral Interbody Fusion System
Baxter Receives FDA Clearance for ALTAPORE Bone Graft
Baxter was granted FDA 510(k) clearance to market ALTAPORE Bioactive Bone Graft as an autograft extender in posterolateral spinal fusion....
Sep 27, 2018, Julie Vetalice
Ethicon’s Skin Closure in Knee Replacement Study
Total knee replacement patients and surgeons reported greater satisfaction with Ethicon's DERMABOND PRINEO Skin Closure System for surgical incisions vs. traditional...
Sep 26, 2018, Julie Vetalice
Gramercy Extremity Orthopedics Receives US Patent for Variable Angle Locking Technology
Gramercy Extremity Orthopedics was awarded U.S. Patent No. 10,058,362 covering a novel approach for Variable Angle Locking Technology....
Sep 26, 2018, Julie Vetalice
OrthoXel Gains FDA Clearance for Apex Femoral Nail
OrthoXel received FDA 510(k) clearance to market the Apex Femoral Nailing System. ...
Sep 26, 2018, Julie Vetalice
4WEB Partners with Tedan, Lattus on Total Lateral Solution
4WEB Medical entered into an exclusive partnership with Lattus Spine and TeDan Surgical Innovations to co-market a turnkey Total Lateral Solution,...
Sep 26, 2018, Julie Vetalice
NuVasive Enrolls Patients in Advanced Materials Science in XLIF Study
NuVasive commenced patient enrollment in a prospective, multicenter U.S. study evaluating advanced spinal implants used in XLIF® procedures....
Sep 26, 2018, Julie Vetalice
SeaSpine Launches Regatta Lateral System
SeaSpine commenced full launch of the Regatta® minimally invasive lateral interbody fusion system....
Sep 26, 2018, Julie Vetalice
CrossRoads Extremity Systems Expands Active Stabilization Portfolio
CrossRoads Extremity Systems launched DynaFORCE® Lapidus plates for tarsometatarsal joint fusion....
Sep 26, 2018, Julie Vetalice
Stryker Gains FDA Clearance for SpineJack Fracture Reduction
Stryker received FDA 510(k) clearance for the SpineJack® implantable reduction system to treat osteoporotic vertebral compression fractures....
Sep 26, 2018, Julie Vetalice
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