DURACON UNICOMPARTMENTAL KNEE SYSTEM— 510(k) K926231

Substantially Equivalent

Howmedica Corp.

FDA 510(k) clearance K926231 for DURACON UNICOMPARTMENTAL KNEE SYSTEM, Substantially Equivalent on 1993-03-30. Applicant: Howmedica Corp..

Clearance details

Applicant: Howmedica Corp.
Product code: Code HSX
Advisory panel: Orthopedic
Date received: 1992-12-11
Decision date: 1993-03-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rutherford, NJ, US

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Adverse events under product code HSX

product code HSX

Injury: 1,003
Other: 1
Total: 1,004

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.