NEUROMED MODEL 1992 LS LAMITRODE LEAD— 510(k) K905255

Substantially Equivalent

Neuromed, Inc.

FDA 510(k) clearance K905255 for NEUROMED MODEL 1992 LS LAMITRODE LEAD, Substantially Equivalent on 1991-01-25. Applicant: Neuromed, Inc..

Clearance details

Applicant: Neuromed, Inc.
Product code: Code GZB
Advisory panel: Neurology
Date received: 1990-11-21
Decision date: 1991-01-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ft. Lauderdale, FL, US

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Adverse events under product code GZB

product code GZB

Death: 4
Injury: 1,879
Other: 2
Total: 1,885

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.