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U.S. Department of Health and Human Services

Product Classification
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Device electrode, spinal epidural
Regulation Description Implanted spinal cord stimulator for pain relief.
Regulation Medical Specialty Neurology
Review Panel Neurology
Product CodeLHG
Premarket Review Office of Neurological and Physical Medicine Devices (OHT5)
Neuromodulation and Physical Medicine Devices (DHT5B)
Submission Type 510(k)
Regulation Number 882.5880
Device Class 2
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
Summary Malfunction
Reporting		 Ineligible
Implanted Device? Yes
Life-Sustain/Support Device? No
Third Party Review Not Third Party Eligible
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