International safety notice

Urgent Field Safety Notice for Algovita Spinal Cord Stimulation System / Clinician Programmer (CP), NUVECTRA

Germany / BfArM · DEU · May 24, 2016

Key facts

Title Urgent Field Safety Notice for Algovita Spinal Cord Stimulation System / Clinician Programmer (CP), NUVECTRA
Regulator Germany / BfArM
Country DEU
Brand Algovita Spinal Cord Stimulation System / Clinician Programmer (CP), NUVECTRA
Manufacturer Urgent Field Safety Notice for Algovita Spinal Cord Stimulation System / Clinician Programmer (CP), NUVECTRA
Models 2016-02, 55449, 10675
Date May 24, 2016
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice
  • 1–9 Matching device models in FDA data

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About International device safety notices

Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.

Source: National medical device regulators (as listed), compiled by Orca1

Browse all International device safety notices