Vericel’s Proposed Public Offering of Common Stock
Vericel intends to sell shares of common stock in an underwritten public offering. Dec 16, 2016
Safe Orthopaedics Receives CE Mark for Oak Pedicle Screw
Safe Orthopaedics received approval under the CE Mark for a next-generation Oak pedicle screw for the treatment of thoracic vertebral fractures. Dec 16, 2016
Study Results: InSpace in the Treatment of Massive Rotator Cuff Tears
Initial study results indicate that patients undergoing the InSpace™ procedure to treat massive rotator cuff tears experienced durable improvements in shoulder function and reductions in shoulder pain at one year. Dec 16, 2016
2016: The Year in Products and Services
Editor’s Note: “Keep me informed on what everyone is doing” is, without fail, one request returned in every ORTHOWORLD Membership... Dec 15, 2016
Study Results: OrthoTrophix TPX-100 in Knee OA
OrthoTrophix announced results of the first proof of principle study of TPX-100 in bilateral knee osteoarthritis, showing improvements at 6 and 12 months in key knee-related outcome measures. Dec 15, 2016
SpinalCyte’s IRB Approval for Phase I Clinical Trial
SpinalCyte received IRB approval to commence Phase I clinical trials with its CybroCell dermal fibroblast cell product in the treatment of degenerative disc disease. Dec 15, 2016
aap Implantate’s New U.S. Distribution Contract for LOQTEQ Products
aap Implantate entered into a distribution contract for LOQTEQ® trauma products with an unnamed U.S. healthcare service provider. Dec 15, 2016
U.K. National Joint Registry Analysis of Zimmer Biomet Trabecular Metal Cups
Zimmer Biomet announced positive outcomes associated with use of Trabecular Metal™ Cups in >9,500 revision hip arthroplasty cases, as reported in data from the National Joint Registry for England, Wales, Northern Ireland and the Isle of Man. Dec 15, 2016
Zimmer Biomet Updates: Product Supply Matters, Form 483
Zimmer Biomet reports that most product lines impacted by previously-disclosed shipping delays have returned to full shipping capacity, and disclosed the receipt of a Form 483 following an FDA inspection of a legacy Biomet manufacturing site in Warsaw, Indiana. Dec 14, 2016
Zimmer Biomet Launches PrimaGen Advanced Allograft
Zimmer Biomet launched PrimaGen Advanced™ Allograft, an autograft substitute comprising cancellous bone + demineralized cortical bone fibers with verified osteoinductivity. Dec 14, 2016
