REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURS— 510(k) K012694

Name: FDA 510(k) clearance K012694
Creator: U.S. Food and Drug Administration
Published: 2002-02-04

Substantially Equivalent

Adven Medical

FDA 510(k) clearance K012694 for REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURS, Substantially Equivalent on 2002-02-04. Applicant: Adven Medical. Device class: 1.

Clearance details

Applicant: Adven Medical
Product code: Code HWE
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 2001-08-14
Decision date: 2002-02-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lubbock, TX, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code HWE

product code HWE

Death: 4
Injury: 448
Malfunction: 19,856
Other: 2
Total: 20,310

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.