SMITH & NEPHEW GLOBAL BIPOLAR SYSTEM— 510(k) K023743

Substantially Equivalent

Smith & Nephew, Inc.

FDA 510(k) clearance K023743 for SMITH & NEPHEW GLOBAL BIPOLAR SYSTEM, Substantially Equivalent on 2003-01-23. Applicant: Smith & Nephew, Inc..

Clearance details

Applicant: Smith & Nephew, Inc.
Product code: Code KWY
Advisory panel: Orthopedic
Date received: 2002-11-07
Decision date: 2003-01-23
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Memphis, TN, US

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Adverse events under product code KWY

product code KWY

Death: 3
Injury: 2,049
Total: 2,052

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.