NuVasive to Resume XLIF Procedures in Japan in 1Q17
NuVasive received Japan regulatory approval for instruments used in the eXtreme Lateral Interbody Fusion (XLIF®) procedure....
NuVasive received Japan regulatory approval for instruments used in the eXtreme Lateral Interbody Fusion (XLIF®) procedure....
Lima Corporate was awarded three new Orthopaedic Data Evaluation Panel ratings for hip implants in the U.K. The ratings are...
AxioMed modified terms of a previously-signed 15-year exclusive license agreement with DSM Biomedical, holder of the patent on polymer technology...
Carevature commenced limited U.S. launch of Dreal™ products for spinal decompression. Full launch is slated for 2017. The system is also...
Intrinsic Therapeutics filed a Premarket Approval application with FDA for the Barricaid® Anular Closure device. ...
ZipLine Medical received China Food and Drug Administration approval of its Zip® Surgical Skin Closure device. ...
CartiHeal received FDA approval of its Investigational Device Exemption application submitted for the Agili-C™ implant, in support of a Premarket Approval application....
Anika Therapeutics received CE Mark approval for ORTHOVISC®-T injection indicated to relieve pain and restore function in tendons affected by chronic...
Providence Medical Technology closed a US $10.5MM new equity financing round. Proceeds will support commercialization and expansion of cervical fusion products....
Conventus Orthopaedics marked the milestone of >700 patients treated with the expandable fracture device, the Conventus Cage™. ...
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