OEM News
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Extremities
Shoulder Innovations Publishes Long Term Data for Inset Glenoid
In the 9+ years follow-up there were no revision surgeries, surgical complications, or infections reported.GlobeNewswire 04.18.19
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Biologics
First Successful Surgeries with Exactech's InterSep Calcium Sulfate Bone Void Filler
InterSep is a 100 percent synthetic calcium sulfate bone void filler that is engineered to fully resorb and replace bone during the healing process.Business Wire 04.17.19
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Software & Quality | Spine/Neurology | Trauma/Sports
Brainlab's Spine & Trauma 3D Navigation Software Recalled Over Misinterpretation Risk
Brainlab is recalling the Spine & Trauma 3D Navigation Software due to the potential for incorrect information to display during surgery.U.S. Food and Drug Administration 04.16.19
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Spine/Neurology
Globus Releases FORTIFY Variable Angle Expandable Corpectomy Spacer System
FORTIFY VA is an expandable corpectomy spacer that optimizes anatomical fit using an anterior cervical or one of several approaches to the thoracolumbar spine.GlobeNewswire 04.16.19
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Extremities | Instruments
In2Bones Launches ClearGuard LE Endoscopic Soft Tissue Release System
The ClearGuard LE System is designed for a variety of soft tissue releases of the lower extremity.GlobeNewswire 04.16.19
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Spine/Neurology
SI-BONE's iFuse Bedrock Spinopelvic Fixation Technology Gains Additional FDA Nod
The company's iFuse Bedrock technology was cleared for fusion of the sacroiliac (SI) joint during long construct procedures.GlobeNewswire 04.15.19
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Trice Medical Appoints New CEO
Mark Foster joined Trice in 2016, serving as VP of global sales and CCO and was promoted to president in March 2018.Business Wire 04.15.19
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Imaging | Software & Quality
FDA OKs Scientific Analytics' Computer-Vision-Powered Motion Analysis Technology
The company also formed a strategic collaboration with Hospital for Special Surgery, which has been ranked #1 in orthopedics for the past 9 years.PR Newswire 04.04.19
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Spine/Neurology
Orthofix Releases Two-Year Data from M6-C Artificial Cervical Disc IDE Study
Presented for the first time during ISASS, the data shows a reduction in pain and opioid medication use.Business Wire 04.04.19
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Smith & Nephew Acquires Developer of Pressure Injury Prevention Device
Deal follows a two-year partnership with Leaf Healthcare as an exclusive distributor and strategic investor.Smith & Nephew plc 04.03.19
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Clemson, Arthrex Begin Program to Train Students for Surgical Device Development
Arthrex will award 10 annual scholarships totaling $75,000 during program’s first year.Tara Romanella, Clemson University 04.03.19
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Spine/Neurology
Intellirod Spine Receives First Ever Spine FDA De Novo Approval
The company received approval for its revolutionary disposable spinal rod strain sensor, the LOADPRO.Business Wire 04.02.19
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Spine/Neurology
NuVasive Proprietary Porous PEEK Technology Used In First XLIF Spine Surgery Cases
Company expands applications of Porous PEEK surface technology to lateral surgery with first-of-its-kind Cohere XLIF implant.PR Newswire 04.01.19
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Spine/Neurology
SpineEX Gains Patent for Expandable and Adjustable Lordosis Interbody Fusion System
The patent covers a novel mechanism that allows surgeons to adjust the posterior and anterior sides of an interbody fusion device independently of one another.GlobeNewswire 03.29.19
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Spine/Neurology
Alphatec Announces Commercial Launch of its First IdentiTi Porous Titanium Interbody System
Product offer implant options that take advantage of bone’s affinity for titanium.Globe Newswire 03.28.19
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Large Joint
First Successful Hip Replacement Surgery Completed With New Alteon Cup and XLE Liner
The Alteon Cup and XLE Liner are the newest additions to Exactech’s Alteon Platform Hip Replacement System.Business Wire 03.27.19
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Biologics
Bioventus Launches OSTEOAMP SELECT Fibers
Fibers are uniquely processed to retain essential growth factors supporting bone formation and the nanotextured fibers provide a conduit for cell migration.Bioventus 03.27.19
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Spine/Neurology
SpineEX Gains Additional FDA Nod for Sagittae Lateral Lumbar Interbody Fusion System
This additional 510(k) clearance will enhance SpineEX’s ability to achieve full-scale commercialization.GlobeNewswire 03.25.19
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MIS/Robotics | Spine/Neurology
FDA OKs Zimmer Biomet's ROSA ONE Spine System for Robotically-Assisted Surgeries
Zimmer Biomet becomes the first company in the world with 510(k) clearance for brain, spine, and knee offerings on one robotic platform.PR Newswire 03.25.19
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Spine/Neurology
First Patient Enrolled in RTI Surgical's FORTE Clinical Study
RTI continues to advance its growing body of clinical evidence for the Fortilink Interbody Fusion Device with TETRAfuse 3D Technology.GlobeNewswire 03.20.19
