CRANIOCUT— 510(k) K022942

Substantially Equivalent

Aesculap, Inc.

FDA 510(k) clearance K022942 for CRANIOCUT, Substantially Equivalent on 2002-10-21. Applicant: Aesculap, Inc..

Clearance details

Applicant: Aesculap, Inc.
Product code: Code HBE
Advisory panel: Neurology
Date received: 2002-09-05
Decision date: 2002-10-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Center Valley, PA, US

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Adverse events under product code HBE

product code HBE

Injury: 306
Malfunction: 7,175
Other: 1
Total: 7,482

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.