MARNE M.T.P.J. ORTHOPEDIC IMPLANT— 510(k) K781380

Name: FDA 510(k) clearance K781380
Creator: U.S. Food and Drug Administration
Published: 1979-02-21

Substantially Equivalent

Farah , Ltd.

FDA 510(k) clearance K781380 for MARNE M.T.P.J. ORTHOPEDIC IMPLANT, Substantially Equivalent on 1979-02-21. Applicant: Farah , Ltd.. Device class: 2.

Clearance details

Applicant: Farah , Ltd.
Product code: Code KYJ
Device class: Class 2
Regulation: 21 CFR 888.3230
Advisory panel: Orthopedic
Date received: 1978-08-11
Decision date: 1979-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code KYJ

product code KYJ

Injury: 210
Total: 210

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.