DEPUY AML HIP PROSTHESIS— 510(k) K061833

Name: FDA 510(k) clearance K061833
Creator: U.S. Food and Drug Administration
Published: 2006-07-17

Substantially Equivalent

DePuy Orthopaedics, Inc.

FDA 510(k) clearance K061833 for DEPUY AML HIP PROSTHESIS, Substantially Equivalent on 2006-07-17. Applicant: DePuy Orthopaedics, Inc.. Device class: 2.

Clearance details

Applicant: DePuy Orthopaedics, Inc.
Product code: Code LPH
Device class: Class 2
Regulation: 21 CFR 888.3358
Advisory panel: Orthopedic
Date received: 2006-06-29
Decision date: 2006-07-17
Decision: Substantially Equivalent
Clearance type: Special
Location: Warsaw, IN, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code LPH

product code LPH

Death: 73
Injury: 31,640
Malfunction: 3,358
Other: 2
Total: 35,073

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.