INTERPORE CROSS INTERNATIONAL ANTERIOR FIXATION DEVICE (AFD)— 510(k) K022143

Substantially Equivalent

Interpore Cross Intl.

FDA 510(k) clearance K022143 for INTERPORE CROSS INTERNATIONAL ANTERIOR FIXATION DEVICE (AFD), Substantially Equivalent on 2003-01-23. Applicant: Interpore Cross Intl..

Clearance details

Applicant: Interpore Cross Intl.
Product code: Code MQP
Advisory panel: Orthopedic
Date received: 2002-07-02
Decision date: 2003-01-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

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Adverse events under product code MQP

product code MQP

Injury: 372
Malfunction: 519
Total: 891

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.