STRYKER INTERVENTIONAL PAIN RF GENERATOR— 510(k) K032601

Name: FDA 510(k) clearance K032601
Creator: U.S. Food and Drug Administration
Published: 2004-04-01

Substantially Equivalent

Valley Forge Scientific Corp.

FDA 510(k) clearance K032601 for STRYKER INTERVENTIONAL PAIN RF GENERATOR, Substantially Equivalent on 2004-04-01. Applicant: Valley Forge Scientific Corp.. Device class: 2.

Clearance details

Applicant: Valley Forge Scientific Corp.
Product code: Code GXD
Device class: Class 2
Regulation: 21 CFR 882.4400
Advisory panel: Neurology
Date received: 2003-08-25
Decision date: 2004-04-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oaks, PA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code GXD

product code GXD

Injury: 228
Total: 228

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.