ADVANCE TOTAL KNEE SYSTEM— 510(k) K061223

Substantially Equivalent

Wrightmedicaltechnologyinc

FDA 510(k) clearance K061223 for ADVANCE TOTAL KNEE SYSTEM, Substantially Equivalent on 2006-08-18. Applicant: Wrightmedicaltechnologyinc.

Clearance details

Applicant: Wrightmedicaltechnologyinc
Product code: Code MBH
Advisory panel: Orthopedic
Date received: 2006-05-02
Decision date: 2006-08-18
Decision: Substantially Equivalent
Clearance type: Special
Location: Arlington, TN, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code MBH

product code MBH

Injury: 6,545
Malfunction: 2,023
Total: 8,568

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.