FEMORAL HEMI-HIP PROSTHESIS— 510(k) K862460

Substantially Equivalent

Orthopaedic Device Corp.

FDA 510(k) clearance K862460 for FEMORAL HEMI-HIP PROSTHESIS, Substantially Equivalent on 1986-10-06. Applicant: Orthopaedic Device Corp..

Clearance details

Applicant: Orthopaedic Device Corp.
Product code: Code KWY
Advisory panel: Orthopedic
Date received: 1986-06-30
Decision date: 1986-10-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Paterson, NJ, US

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Adverse events under product code KWY

product code KWY

Death: 3
Injury: 2,049
Total: 2,052

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.