ANGIOTECH CVC— 510(k) K073520

Name: FDA 510(k) clearance K073520
Creator: U.S. Food and Drug Administration
Published: 2008-04-11

Substantially Equivalent

Angiotech Pharmaceuticals, Inc.

FDA 510(k) clearance K073520 for ANGIOTECH CVC, Substantially Equivalent on 2008-04-11. Applicant: Angiotech Pharmaceuticals, Inc.. Device class: 2.

Clearance details

Applicant: Angiotech Pharmaceuticals, Inc.
Product code: Code FOZ
Device class: Class 2
Regulation: 21 CFR 880.5200
Advisory panel: General Hospital
Date received: 2007-12-14
Decision date: 2008-04-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Herndon, VA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code FOZ

product code FOZ

Death: 38
Injury: 2,290
Malfunction: 25,858
Other: 11
Total: 28,197

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.