Julie A. Vetalice, Author at ORTHOWORLD

Centinel Spine Gains FDA Clearance of FLX 3D Printed Titanium Interbodies

Centinel Spine received FDA 510(k) clearance to market the FLX platform of Integrated Interbody and non-integrated interbody fusion devices.

Jun 08, 2018

K2M achieved the milestone of its 100th product following FDA 510(k) clearance and launch of the OZARK Cervical Plate.

Jun 07, 2018

3D-Side received a ‚¬3MM capital increase to support launch of Customize, a web-based SaaS for mass customization of medical devices.

Jun 07, 2018

Ziptek marked the first U.S. implantation of the ZipE® resorbable knotless suture button.

Jun 06, 2018

EOS imaging received FDA 510(k) clearance to market hipEOS 3.0 surgical planning software for THA.

Jun 06, 2018

OrthAlign realized the clinical milestone of its 2,000th case with HipAlign® handheld navigation for Direct Anterior Total Hip Replacement.

Jun 06, 2018

Vericel closed its underwritten public offering of 5,750,000 shares of is common stock for $13/share, for gross proceeds of ~US $74.8MM.

Jun 06, 2018

Diamond Orthopedic received FDA 510(k) clearance for sterile packaged faceted bone screws.

Jun 05, 2018

OrthoPediatrics announced the first surgery utilizing the Pediatric Nailing Platform | FEMUR rigid IM nail.

Jun 05, 2018

CoreLink has acquired Expanding Orthopedics, developer of the FLXfit line of expanding interbody devices. Terms were not disclosed.

Jun 05, 2018