K2M Expands MESA Platform with FDA Clearance for Growing Spine Application
K2M received FDA 510(k) clearance for components for the MESA® Spinal System, supporting use as part of a growing rod...
Sep 21, 2016,
K2M Expands MESA Platform with FDA Clearance for Growing Spine Application
Study Results from Inspired Spine’s MIS Direct Thoracic Interbody Fusion Procedure
Study results indicate that the minimally invasive direct thoracic interbody fusion or MIS-DTIF approach, offered by Inspired Spine, was shown...
Sep 21, 2016, Julie Vetalice
Spineart Secures Investment
Spineart secured a 30MM (~US $33MM) investment. Proceeds will support sales, geographical expansion in markets such as the U.S. and Europe and...
Sep 20, 2016, Julie Vetalice
Zimmer Biomet Launches VANGUARD Individualized Design Knee
Zimmer Biomet launched the Vanguard® Individualized Design total knee construct, offering two individual polyethylene bearings with different articulations to support a...
Sep 20, 2016, Julie Vetalice
First Surgery with Band-LOK Pedicle-Sparing Polyester Band Technology
Band-LOK announced completion of the first spinal surgery using its pedicle-sparing polyester band technology....
Sep 20, 2016, Julie Vetalice
First Clinical Uses of Integra LifeScience’s Cadence Total Ankle in Europe
Integra LifeSciences announced successful completion of initial procedures using the Cadence™ Total Ankle in Europe....
Sep 20, 2016, Julie Vetalice
Life Spine Receives FDA Clearance of PRO-LINK Ti Standalone Cervical Spacer
Life Spine received FDA 510(k) clearance to market the PRO-LINK® Ti Standalone Cervical Spacer. Full launch is scheduled for the end of...
Sep 20, 2016, Julie Vetalice
OSTEOGROW Research Update
OSTEOGROW, an EU-funded collaborative research project, is investigating a new bone regeneration therapy based on autologous blood + BMP-6 for use...
Sep 19, 2016, Julie Vetalice
RTI Surgical Receives Regulatory Clearances for nanOss Bioactive in Australia, Europe
RTI Surgical received regulatory clearance for nanOss® Bioactive bone void filler in Australia, as well as CE Mark for nanOss Bioactive Loaded and...
Sep 19, 2016, Julie Vetalice
NuVasive Receives FDA 510(k) Clearance to Market MAGEC System
NuVasive Specialized Orthopedics received FDA 510(k) clearance to market the MAGEC® system for treatment of severe spinal deformity....
Sep 19, 2016, Julie Vetalice
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