DCW MODULAR PROXIMAL FEMORAL SYSTEM— 510(k) K904028

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.

Clearance details

Applicant: Dow Corning Wright
Product code: Code LZO
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

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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.