Nuvectra
Nuvectra appears in FDA public data with 2 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-0781-2017, Class II) was initiated on October 11, 2016.
Summary
- Total Recalls
- 2
- 510(k) Clearances
- 0
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-0781-2017 | Class II | Algovita Spinal Cord Stimulation System, Percutaneous Leads, 8-Electrode Percutaneous Lead Kit; | October 11, 2016 |
| Z-1600-2016 | Class II | Nuvectra, Algovita Spinal Cord Stimulation System Clinical Programmer, Model 4500. For use with Algo | April 6, 2016 |