Captus Vascular Retrieval System— 510(k) K170987

Name: FDA 510(k) clearance K170987
Creator: U.S. Food and Drug Administration
Published: 2017-08-28

Substantially Equivalent

Avantec Vascular Corporation

FDA 510(k) clearance K170987 for Captus Vascular Retrieval System, Substantially Equivalent on 2017-08-28. Applicant: Avantec Vascular Corporation. Device class: 2.

Clearance details

Applicant: Avantec Vascular Corporation
Product code: Code MMX
Device class: Class 2
Regulation: 21 CFR 870.5150
Advisory panel: Cardiovascular
Date received: 2017-04-03
Decision date: 2017-08-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sunnyvale, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code MMX

product code MMX

Death: 3
Total: 3

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.