AMK LANDMARK REVISION KNEE FULL WEDGE TIBIAL TRAY— 510(k) K925837

Name: FDA 510(k) clearance K925837
Creator: U.S. Food and Drug Administration
Published: 1994-01-07

Substantially Equivalent for Some Indications

Depuy, Inc.

FDA 510(k) clearance K925837 for AMK LANDMARK REVISION KNEE FULL WEDGE TIBIAL TRAY, Substantially Equivalent for Some Indications on 1994-01-07. Applicant: Depuy, Inc.. Device class: 2.

Clearance details

Applicant: Depuy, Inc.
Product code: Code JWH
Device class: Class 2
Regulation: 21 CFR 888.3560
Advisory panel: Orthopedic
Date received: 1992-11-18
Decision date: 1994-01-07
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Warsaw, IN, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code JWH

product code JWH

Death: 26
Injury: 51,564
Malfunction: 9,725
Other: 9
Total: 61,324

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.