STRYKER MAESTRO SYSTEM— 510(k) K041754

Substantially Equivalent

Stryker Corp.

FDA 510(k) clearance K041754 for STRYKER MAESTRO SYSTEM, Substantially Equivalent on 2004-09-07. Applicant: Stryker Corp..

Clearance details

Applicant: Stryker Corp.
Product code: Code HBB
Advisory panel: Neurology
Date received: 2004-06-29
Decision date: 2004-09-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kalamazoo, MI, US

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Adverse events under product code HBB

product code HBB

Malfunction: 2,656
Total: 2,656

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.