Medicrea Announces FDA Clearance of PASS TULIP Top-Loading Spinal Fixation
Medicrea received FDA 510(k) clearance and performed first surgeries with PASS® TULIP top-loading fixation....
Jun 19, 2017,
Medicrea Announces FDA Clearance of PASS TULIP Top-Loading Spinal Fixation
Medicrea Receives FDA Clearance for UNiD HUB Digital Portal
Medicrea received FDA 510(k) clearance for UNiD™ HUB, a data-driven digital portal that employs Adaptive Spine Intelligence for surgical planning....
Jun 19, 2017, Julie Vetalice
Meditech Spine Receives FDA Clearance for Talos Lumbar PEEK Devices
Meditech Spine received FDA 510(k) clearance for Talos® Lumbar PEEK IBF devices enhanced with hydroxyapatite....
Jun 19, 2017, Julie Vetalice
Medovex Receives First Commercial Orders for DenerveX System
Medovex received its first 3 commercial orders for the DenerveX™ system from distributors in Germany, Italy and the U.K. ...
Jun 19, 2017, Julie Vetalice
GE Additive and Stryker Enter Additive Manufacturing Partnership
GE Additive and Stryker established an agreement to support Stryker’s growth in additive manufacturing, covering new machines, materials and services. ...
Jun 14, 2017, Julie Vetalice
Cretex Companies Acquires Quality Tech Services, Supplier of Outsourced Packaging
Cretex Companies acquired Quality Tech Services, supplier of outsourced packaging for the medical device industry....
Jun 14, 2017, Julie Vetalice
First KneeAlign Total Knee Arthroplasty Cases in Greece
OrthAlign entered the market in Greece with initial KneeAlign® cases completed for alignment and positioning in total knee arthroplasty. ...
Jun 13, 2017, Julie Vetalice
ConforMIS Retrospective Study: Customized vs. Off the Shelf Total Knees
Retrospective study results indicate lower adverse events, more rapid discharge, lower follow-up care costs, etc. with custom knee implants vs....
Jun 13, 2017, Julie Vetalice
SI-BONE Receives FDA Clearance for iFuse-3D
SI-BONE received FDA 510(k) clearance and commenced full U.S. launch of the iFuse-3D™ Implant....
Jun 13, 2017, Julie Vetalice
Vertera Spine Receives CMS ICD-10 Code for COHERE Cervical Interbody Fusion Device
CMS issued a new ICD-10 code for a radiolucent porous interbody fusion device, supporting Vertera Spine’s COHERE cervical device. ...
Jun 13, 2017, Julie Vetalice
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