ARTHROSCOPIC LEG HOLDER— 510(k) K811861

Substantially Equivalent

Stryker Corp.

FDA 510(k) clearance K811861 for ARTHROSCOPIC LEG HOLDER, Substantially Equivalent on 1981-07-16. Applicant: Stryker Corp..

Clearance details

Applicant: Stryker Corp.
Product code: Code HRX
Advisory panel: Orthopedic
Date received: 1981-07-01
Decision date: 1981-07-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code HRX

product code HRX

Injury: 623
Malfunction: 11,257
Total: 11,880

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.