NuVasive SpineTRACK Registry Reaches 10,000 Enrollment Milestone
NuVasive's SpineTRACK Registry reached a milestone of 10,000 patients enrolled since its inception in 2011. ...
May 24, 2018,
Spine
ORTHOFLASHSpinal Elements Expands Launch of Clutch Interspinous Process Device
Spinal Elements commenced full launch of the Clutch® interspinous process device for treatment of various posterior thoracolumbar pathologies....
May 24, 2018, Julie Vetalice
Medacta Launches Customizable MySpine MC Surgical Guides
Medacta announced FDA 510(k) clearance and launch of the MySpine Midline Cortical Pedicle Screw Placement Guide....
May 24, 2018, Julie Vetalice
Implanet Launches JAZZ Evo® for Adult Degenerative Spine Disease
Implanet launched JAZZ Evo® for adult vertebral fusion. The device is the first in a new range of JAZZ® connectors....
May 23, 2018, Julie Vetalice
Life Spine Gains FDA Clearance for PRO-LINK Ti Stand-Alone Cervical Spacer
Life Spine received FDA 510(k) clearance to market additional indications for the PRO-LINK® Ti Stand-Alone Cervical Spacer....
May 23, 2018, Julie Vetalice
Wenzel Spine Announces Case Study of VariLift-LX System
Wenzel Spine announced publication of a case series detailing endoscopic transforaminal decompression and fusion with the VariLift-LX system....
May 23, 2018, Julie Vetalice
Zimmer Biomet Gains 510(k) Clearance for Zyston Strut Open Titanium Interbody Spacer
Zimmer Biomet received FDA 510(k) clearance to market the Zyston® Strut Open Titanium Interbody Spacer, the company's first 3D-printed titanium spinal implant....
May 23, 2018, Julie Vetalice
Cerapedics Study Results: i-FACTOR Bone Graft in Lumbar Posterolateral Spine
Study results indicate that Cerapedics' i-FACTOR Peptide Enhanced Bone Graft demonstrated a 50% fusion rate in lumbar posterolateral spine surgery patients vs. 20%...
May 22, 2018, Julie Vetalice
Providence Medical Technology Gains FDA Clearance for DTRAX Spinal System
Providence Medical Technology announced FDA 510(k) clearance to market its DTRAX® system for use in posterior cervical fusion....
May 22, 2018, Julie Vetalice
Xtant Medical Expands Cervical Portfolio with First Porous Titanium Implant
Xtant Medical received FDA 510(k) clearance for its InTice-C Porous Titanium Cervical Interbody System....
May 22, 2018, Julie Vetalice
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