DCW MODULAR DISTAL FEMORAL SYSTEM— 510(k) K910596

Name: FDA 510(k) clearance K910596
Creator: U.S. Food and Drug Administration
Published: 1991-05-29

Substantially Equivalent

Dow Corning Wright

FDA 510(k) clearance K910596 for DCW MODULAR DISTAL FEMORAL SYSTEM, Substantially Equivalent on 1991-05-29. Applicant: Dow Corning Wright. Device class: 2.

Clearance details

Applicant: Dow Corning Wright
Product code: Code KRO
Device class: Class 2
Regulation: 21 CFR 888.3510
Advisory panel: Orthopedic
Date received: 1991-02-12
Decision date: 1991-05-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arlington, TN, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code KRO

product code KRO

Death: 19
Injury: 4,841
Total: 4,860

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.