DISPOSABLE PERFORATOR— 510(k) K924242

Substantially Equivalent

Codman & Shurtleff, Inc.

FDA 510(k) clearance K924242 for DISPOSABLE PERFORATOR, Substantially Equivalent on 1993-07-08. Applicant: Codman & Shurtleff, Inc..

Clearance details

Applicant: Codman & Shurtleff, Inc.
Product code: Code HBF
Advisory panel: Neurology
Date received: 1992-08-24
Decision date: 1993-07-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Randolph, 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.