MAUDE manufacturer profile

UNKNOWN · LGW

MAUDE profile for Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

Key facts

Manufacturer UNKNOWN
Manufacturer group UNKNOWN
Product code LGW
Product code name Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

At a glance

  • 10–99 MAUDE reports
  • 1–9 Death reports
  • 10–99 Injury reports
  • 10–99 Malfunction reports
  • 10–99 Problems flagged by Orca1 signal analytics
  • Insufficient Information, Therapeutic or Diagnostic Output Failure, Failure of Implant, Adverse Event Without Identified Device or Use Problem, No Clinical Signs, Symptoms or Conditions, Inadequate Pain Relief, Pain, Ambulation Difficulties Most reported problems

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

About MAUDE manufacturer and product code profiles

Manufacturer profiles aggregate MAUDE reports for one manufacturer within one product code, the level at which device safety signals are usually reviewed.

Source: U.S. Food and Drug Administration (FDA), MAUDE database; aggregation by Orca1

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