DCW MODULAR PROXIMAL FEMORAL SYSTEM— 510(k) K904028

Name: FDA 510(k) clearance K904028
Creator: U.S. Food and Drug Administration
Published: 1991-01-14

Substantially Equivalent for Some Indications

Dow Corning Wright

FDA 510(k) clearance K904028 for DCW MODULAR PROXIMAL FEMORAL SYSTEM, Substantially Equivalent for Some Indications on 1991-01-14. Applicant: Dow Corning Wright. Device class: 2.

Clearance details

Applicant: Dow Corning Wright
Product code: Code LZO
Device class: Class 2
Regulation: 21 CFR 888.3353
Advisory panel: Orthopedic
Date received: 1990-08-31
Decision date: 1991-01-14
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Arlington, TN, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code LZO

product code LZO

Death: 17
Injury: 12,942
Malfunction: 1,756
Total: 14,715

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.