CODMAN DISPOSABLE PERFORATOR, MODEL(S) 26-1222, 26-1223— 510(k) K071931

Substantially Equivalent

Codman & Shurtleff, Inc.

FDA 510(k) clearance K071931 for CODMAN DISPOSABLE PERFORATOR, MODEL(S) 26-1222, 26-1223, Substantially Equivalent on 2007-10-22. Applicant: Codman & Shurtleff, Inc..

Clearance details

Applicant: Codman & Shurtleff, Inc.
Product code: Code HBF
Advisory panel: Neurology
Date received: 2007-07-13
Decision date: 2007-10-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Raynham, MA, US

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Adverse events under product code HBF

product code HBF

Injury: 587
Malfunction: 621
Other: 1
Total: 1,209

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.