AXIEM IMAGELESS HIP MODULE FOR THE STEALTHSTATION SYSTEM— 510(k) K061248

Substantially Equivalent

Medtronic Navigation, Inc.

FDA 510(k) clearance K061248 for AXIEM IMAGELESS HIP MODULE FOR THE STEALTHSTATION SYSTEM, Substantially Equivalent on 2006-08-31. Applicant: Medtronic Navigation, Inc..

Clearance details

Applicant: Medtronic Navigation, Inc.
Product code: Code HAW
Advisory panel: Neurology
Date received: 2006-05-03
Decision date: 2006-08-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Louisville, CO, US

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Adverse events under product code HAW

product code HAW

Death: 52
Injury: 1,083
Malfunction: 17,300
Total: 18,435

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.