Bioactive Glass Shown Effective Towards Antibiotic-resistant Bacteria
Studies of BonAlive® indicate that the naturally-antibacterial bioactive glass yields excellent results in the treatment of osteomyelitis, without the use of...
Mar 08, 2017,
Bioactive Glass Shown Effective Towards Antibiotic-resistant Bacteria
Vertiflex Completes $40 Million Financing Round
Vertiflex will use funds from a US $40MM financing round to support U.S. commercial expansion of the Superion® Indirect Decompression System....
Mar 08, 2017, Julie Vetalice
Study Results: Vitrium Bioactive Glass in Ovine Spinal Fusion
Results from ovine study of Bio2 Technologies’ Vitrium bioactive glass demonstrated the device’s capability to support interbody fusion....
Mar 08, 2017, Julie Vetalice
Study Results: Use of CT Imaging in Post-op Assessment of Spine Surgery
Studies found that prevalence of CT imaging following complex spine surgery grew more than 2-fold from 6 months to 5...
Mar 08, 2017, Julie Vetalice
Three New Ex-U.S. Distribution Partners for VTI
Vertebral Technologies appointed new distributors in Finland, Germany and Sweden to expand access to InterFuse® modular interbody fusion implants....
Mar 07, 2017, Julie Vetalice
Distribution Agreement for BoneScalpel in China
Misonix entered into an exclusive agreement with Weigao Orthopedic for distribution of the BoneScalpel in China, Hong Kong and Macau....
Mar 07, 2017, Julie Vetalice
FDA Clearance for intellijoint HIP Anterior Application
Intellijoint Surgical received FDA 510(k) clearance to market the intellijoint HIP® Anterior application for surgical navigation....
Mar 07, 2017, Julie Vetalice
Vertos Medical mild Procedure Receives Broad Coverage Under Medicare
Vertos Medical received broad U.S. Medicare coverage for mild®, a procedure for the treatment of lumbar spinal stenosis....
Mar 07, 2017, Julie Vetalice
Full Commercial Launch of UniAlign
OrthAlign commenced full commercial launch of UniAlign™, the first handheld surgical navigation device for unicompartmental knee arthroplasty....
Mar 06, 2017, Julie Vetalice
FDA 510(k) Clearance for NanoFUSE BA
Amend Surgical received FDA 510(k) clearance to market NanoFUSE® BA as a bone graft extender for spine and orthopaedic applications....
Mar 02, 2017, Julie Vetalice
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