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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 the device name listed in this FDA 510(k) record. The listed applicant is Avantec Vascular Corporation. It received FDA 510(k) clearance on 2017-08-28 under 510(k) 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. The listed applicant is Avantec Vascular Corporation. The 510(k) number is K170987.

When did Captus Vascular Retrieval System receive FDA 510(k) clearance?

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

Who is the listed applicant for Captus Vascular Retrieval System?

The FDA 510(k) record lists Avantec Vascular Corporation as the applicant. This does not by itself establish the device manufacturer.

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

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

Other records listing Avantec Vascular Corporation as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K251207Sangria™ Thrombectomy System

Related Devices (Code: MMX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K242776LimFlow V-CeiverLimFlow, Inc.K241259Amplatz Goose Neck Snare KitMedtronic, Inc.K232443Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval KitArgon Medical Devices, Inc.K222254Gunther Tulip Vena Cava Filter Retrieval SetCook IncorporatedK222083LimFlow V-CeiverLimFlow, Inc.K212988ONO Retrieval DeviceOnocor Vascular, LLC

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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