K102172

Substantially Equivalent

MSA HIP SYSTEM

Applicant: Global Manufacturing Technology
Product code: MEH
Advisory panel: Orthopedic
Date received: 2010-08-02
Decision date: 2011-03-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Adverse events under product code MEH

product code MEH

Injury: 2,021
Total: 2,021

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.