CODMAN CRANIOSORB ABSORBABLE FIXATION SYSTEM— 510(k) K992905

Substantially Equivalent

Codman & Shurtleff, Inc.

FDA 510(k) clearance K992905 for CODMAN CRANIOSORB ABSORBABLE FIXATION SYSTEM, Substantially Equivalent on 2000-08-01. Applicant: Codman & Shurtleff, Inc..

Clearance details

Applicant: Codman & Shurtleff, Inc.
Product code: Code JEY
Advisory panel: Dental
Date received: 1999-08-30
Decision date: 2000-08-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Raynham, MA, US

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Adverse events under product code JEY

product code JEY

Injury: 1,542
Malfunction: 2,292
Total: 3,834

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.