Regulatory Spine Intertek Issues First UL 2900-2-1 Certification to Medical Device Manufacturer NuVasive, Inc. byChris StewartMarch 8, 2022
Regulatory Spine Top Stories NuVasive Receives Latest FDA 510(k) Clearance for Pulse Platform and Announces Commercial Launch byChris StewartJuly 30, 2021
Spine Top Stories NuVasive Launches Pulse™-The First Integrated Technology Platform to Enable Better Spine Surgery byChris StewartJuly 10, 2019
