STELKAST UNICONDYLAR KNEE SYSTEM— 510(k) K032824

Substantially Equivalent

Stelkast Company

FDA 510(k) clearance K032824 for STELKAST UNICONDYLAR KNEE SYSTEM, Substantially Equivalent on 2003-11-13. Applicant: Stelkast Company.

Clearance details

Applicant: Stelkast Company
Product code: Code HSX
Advisory panel: Orthopedic
Date received: 2003-09-10
Decision date: 2003-11-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mcmurray, PA, 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.