comparemela.com

Latest Breaking News On - ப்ரிஸிஶந் முதுகெலும்பு இன்க் - Page 1 : comparemela.com

Global Osteosynthesis Devices Market (2020 to 2027) - Market Trajectory & Analytics

Global Osteosynthesis Devices Market (2020 to 2027) - Market Trajectory & Analytics
apnews.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from apnews.com Daily Mail and Mail on Sunday newspapers.

Precision Spine® Reaches Milestone with the Reform® Modular Pedicle Screw System

® Modular Pedicle Screw System, first introduced by Precision Spine in April 2016, today reaches a monumental milepost, its 30,000 th modular screw implantation. This historic milestone is most impressive when highlighted by the fact that there have been no reported dissociations to date. The Reform ® Modular Pedicle Screw System provides surgeons with increased flexibility, versatility, and visibility to meet the varying requirements of degenerative and trauma procedures. The cobalt chrome and titanium tulips are available in both 5.5 and 4.75mm sizes, with standard and reduction options. The system features Tru-Lock Technology that allows the tulip to be attached with a consistent attachment force, as well as a helpful audible click and tactile feel to confirm attachment. The titanium modular cannulated and non-cannulated screws feature a minimally tapered, triple lead thread, as well as a self-starting aggressive screw tip and enlarged T25 drive feature ─ the combination of

Spinal Fusion Devices Market 2021 – Global Share, Growth, Outlook, Size, Opportunities, Trends, Regi

Spinal Fusion Devices Market 2021 – Global Share, Growth, Outlook, Size, Opportunities, Trends, Regi
pharmiweb.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from pharmiweb.com Daily Mail and Mail on Sunday newspapers.

Precision Spine® Receives FDA 510(K) Clearance for the Dakota ACDF™ Standalone System

Press release content from Business Wire. The AP news staff was not involved in its creation. Precision Spine® Receives FDA 510(K) Clearance for the Dakota ACDF™ Standalone System February 4, 2021 GMT PARSIPPANY, N.J. (BUSINESS WIRE) Feb 4, 2021 Precision Spine, Inc., a medical device company dedicated to Made-in-the-USA manufacturing, announced today that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for the Dakota ACDF™ Standalone System in the treatment of degenerative disc disease (DDD). The Dakota ACDF system features a titanium plate polyetheretherketone (PEEK) cage with cortical cancellous screws for maximum support and a generous cavity for autogenous bone graft to help facilitate fusion.

© 2024 Vimarsana

vimarsana © 2020. All Rights Reserved.