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Bard Snare Retrieval Kit

by Neometrics, Inc.

510(k) K152560

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 6 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 6 Oct 2026. What this means

Regulatory status

as of registry sync 6 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK152560 Date23 Oct 2015ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 6 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
MMX
Device Class
Class II
Regulation
21 CFR Part 870.5150
Advisory Committee
Cardiovascular
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 27 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The Bard Snare Retrieval Kit is a percutaneous retrieval device used to remove Bard optional vena cava filters with a retrieval hook. It features kink-resistant nitinol construction, a radiopaque loop for visibility, and a marker band for accurate placement.

This device is supplied as a single-use kit and is intended for percutaneous procedures. It has received FDA 510(k) clearance with the product code MMX and is classified as a Class II device. The kit is designed for use in cardiovascular procedures and is manufactured by Neometrics, Inc.

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Questions

AI-generated answers, 27 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

  • What is the Bard Snare Retrieval Kit used for?

    The Bard Snare Retrieval Kit is a percutaneous retrieval device specifically designed to remove Bard optional vena cava filters using a retrieval hook. It is intended for use in cardiovascular procedures.

  • How is the Bard Snare Retrieval Kit supplied?

    The Bard Snare Retrieval Kit is supplied as a single-use kit for percutaneous procedures. It features kink-resistant nitinol construction, a radiopaque loop for visibility, and a marker band for accurate placement during use.

  • What is the regulatory status of the Bard Snare Retrieval Kit?

    The Bard Snare Retrieval Kit has received FDA 510(k) clearance with the product code MMX and is classified as a Class II device. It was cleared through the traditional pathway with a decision of substantial equivalence.

  • Who manufactures the Bard Snare Retrieval Kit?

    The Bard Snare Retrieval Kit is manufactured by Neometrics, Inc., located in Plymouth, Minnesota. The company has been responsible for the design and production of this cardiovascular device.