Medicrea Announces First MIS Spine Surgery with Patient-Specific Implants
Medicrea announced completion of the world’s first minimally invasive spine procedure using patient-specific implants, with the UNiD™ MIS Rod....
Aug 01, 2017,
Medicrea Announces First MIS Spine Surgery with Patient-Specific Implants
Integra LifeSciences 2Q17 Orthopaedic Revenue
ORTHOWORLD estimates Integra LifeSciences’ 2Q17 orthopaedic revenue at US $37.3MM, +34.1% from 2Q16, and 1H17 revenue of $68.5MM, +27.1% vs....
Aug 01, 2017, Julie Vetalice
OrthAlign Enters Distribution Partnership in Panama
OrthAlign announced first KneeAlign® total knee arthroplasties completed in Panama, alongside entrance into a distribution partnership with Ortosistemas....
Jul 31, 2017, Julie Vetalice
Anika Therapeutics Posts Orthobiologics Sales Growth for 2Q17/1H17
Anika Therapeutics posted 2Q17 orthobiologic revenue of US $24.5MM, +5.0% vs. 2Q16, and 1H17 revenue of $44.7MM, +4.2% vs. 1H16....
Jul 31, 2017, Julie Vetalice
First US Surgeries with 4WEB 3D-Printed Lateral Spine Truss
4WEB Medical announced first surgeries with its Lateral Spine Truss interbody fusion device....
Jul 28, 2017, Julie Vetalice
ConMed Reports 2Q17 Revenue
ConMed posted 2Q17 arthroscopy/soft tissue repair revenue of US $105.5MM, -0.3% vs. 2Q16....
Jul 28, 2017, Julie Vetalice
Camber Spine Exceeds 150th Implantation of ENZA Zero-Profile ALIF
Camber Spine Technologies has surpassed 150 implantations of its ENZA™ Zero-Profile ALIF device at one year following launch....
Jul 27, 2017, Julie Vetalice
CTL Medical Receives FDA 510(k) Clearance for MATISSE ACIF Cage
CTL Medical received FDA 510(k) clearance to market the MATISSE™ titanium ACIF cage....
Jul 26, 2017, Julie Vetalice
Australia Regulatory Approval for Providence Medical’s DTRAX Cervical Fusion Devices
Providence Medical Technology was granted regulatory approval in Australia for DTRAX® cervical fusion devices....
Jul 25, 2017, Julie Vetalice
Vertera Spine Receives FDA 510(k) for COALESCE PEEK LIF Device
Vertera Spine received FDA 510(k) clearance to market the COALESCE™ interbody fusion device for ALIF, TLIF, PLIF and LLIF procedures. ...
Jul 25, 2017, Julie Vetalice
Loading new posts...
No more posts
