Life Spine’s First Clinical Cases with PROLIFT Post Pack Expandable Interbody
Initial clinical cases have been performed with Life Spine's PROLIFT® Post Pack expandable interbody system....
Oct 30, 2018,
Spine
ORTHOFLASHAurora Spine Granted EU Patent for ZIP Minimally Invasive Spinal Devices
Aurora Spine was granted an EU Patent covering ZIP® interspinous devices....
Oct 25, 2018, Julie Vetalice
OrthoPediatrics Gains FDA Clearance for Small Stature Scoliosis System
OrthoPediatrics received FDA 510(k) clearance to market the RESPONSE 4.5/5.0mm system to treat complex scoliosis in smaller stature patients....
Oct 19, 2018, Julie Vetalice
VISEON Gains FDA Clearance for Voyant Surgical Platform
Viseon received FDA 510(k) clearance to market the Voyant System for Minimally Invasive Spine Surgery access, visualization and illumination. ...
Oct 18, 2018, Julie Vetalice
K2M Expands MESA Platform with FDA Clearance for Sagittal Imbalance Application
K2M received additional FDA 510(k) clearance for the MESA® Spinal System, supporting use of sagittal plane correction in idiopathic scoliosis....
Oct 11, 2018, Julie Vetalice
SpineEX Gains FDA Clearance for Sagittae LLIF
SpineEX received FDA 510(k) clearance to market its Sagittae® expandable device for minimally invasive lateral lumbar interbody fusion. ...
Oct 10, 2018, Julie Vetalice
ApiFix System Reaches 250-Patient Milestone in Scoliosis Correction
The ApiFix Minimally Invasive Deformity Correction (MID-C) technology for correction of Adolescent Idiopathic Scoliosis has been used in 250 patients...
Oct 04, 2018, Julie Vetalice
SI-BONE Announces UK Guidance Recommendation for iFuse
The U.K.'s National Institute for Health and Care Excellence published medical technology guidance recommending SI-BONE's iFuse® for the treatment of chronic sacroiliac joint pain....
Oct 03, 2018, Julie Vetalice
Vertos Medical Enrolls in New MOTION Study of MILD Procedure
Vertos Medical enrolled the first patient into MOTION, a new multicenter two-year U.S. study of the mild® outpatient procedure for...
Oct 01, 2018, Julie Vetalice
FDA Approves Update of Mobi-C Cervical Disc Labeling to Include 7-Year Clinical Results
FDA approved an update to the labeling for Zimmer Biomet's Mobi-C® Cervical Disc to include 7-year clinical results, showing the...
Sep 28, 2018, Julie Vetalice
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