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FDA 510(k)

Captus Vascular Retrieval System

K-Number: K170987 · 2017-08-28

ApplicantAvantec Vascular Corporation
Decision Date2017-08-28
Product CodeMMX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Captus Vascular Retrieval System is a medical device manufactured by Avantec Vascular Corporation. It received FDA 510(k) clearance on 2017-08-28 under approval number K170987. The device is classified under product code MMX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Captus Vascular Retrieval System?

Captus Vascular Retrieval System is a medical device that received FDA 510(k) clearance on 2017-08-28. It is manufactured by Avantec Vascular Corporation. The 510(k) number is K170987.

When was Captus Vascular Retrieval System approved by the FDA?

Captus Vascular Retrieval System received FDA 510(k) clearance on 2017-08-28, under approval number K170987.

What company makes Captus Vascular Retrieval System?

Captus Vascular Retrieval System is manufactured by Avantec Vascular Corporation.

What is the FDA product code for Captus Vascular Retrieval System?

The FDA product code for Captus Vascular Retrieval System is MMX.

Related Clinical Trials

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Related PubMed Literature

PMID: 40258332 Chronic expanding hematoma following Gamma Knife irradiation for primary central nervous system lymphoma: illustrative case. Journal of neurosurgery. Case lessons (2025)

Other Devices by Avantec Vascular Corporation

K251207Sangria™ Thrombectomy System

Related Devices (Code: MMX)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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