LHG

1 FDA 510(k) clearances · Product code

FDA profile

Official device name

Electrode, Spinal Epidural

Device class

Class II (moderate risk)

Regulation

21 CFR 882.5880

Medical specialty

Neurology

Flags

Implant

Adverse events (MAUDE)

1992: 3 · 1993: 1 · 1997: 2 · 1998: 6 · 1999: 1
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.

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