Nuvectra

FDA Regulatory Profile

Summary

Total Recalls
2
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-0781-2017Class IIAlgovita Spinal Cord Stimulation System, Percutaneous Leads, 8-Electrode Percutaneous Lead Kit; October 11, 2016
Z-1600-2016Class IINuvectra, Algovita Spinal Cord Stimulation System Clinical Programmer, Model 4500. For use with AlgoApril 6, 2016