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FDA 510(k)

MEDTRONIC CLEAR INTRAVACULAR ARTERIOTOMY SHUNT

K-Number: K120612 · 2012-05-25

ApplicantMedtronic, Inc.
Decision Date2012-05-25
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDTRONIC CLEAR INTRAVACULAR ARTERIOTOMY SHUNT is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic, Inc.. It received FDA 510(k) clearance on 2012-05-25 under 510(k) number K120612. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDTRONIC CLEAR INTRAVACULAR ARTERIOTOMY SHUNT?

MEDTRONIC CLEAR INTRAVACULAR ARTERIOTOMY SHUNT is a medical device that received FDA 510(k) clearance on 2012-05-25. The listed applicant is Medtronic, Inc.. The 510(k) number is K120612.

When did MEDTRONIC CLEAR INTRAVACULAR ARTERIOTOMY SHUNT receive FDA 510(k) clearance?

MEDTRONIC CLEAR INTRAVACULAR ARTERIOTOMY SHUNT received FDA 510(k) clearance on 2012-05-25, under 510(k) number K120612.

Who is the listed applicant for MEDTRONIC CLEAR INTRAVACULAR ARTERIOTOMY SHUNT?

The FDA 510(k) record lists Medtronic, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDTRONIC CLEAR INTRAVACULAR ARTERIOTOMY SHUNT?

The FDA product code for MEDTRONIC CLEAR INTRAVACULAR ARTERIOTOMY SHUNT is DWF.

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Related Devices (Code: DWF)

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.

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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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