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FDA 510(k)

CXI TriForce Peripheral Crossing Set

K-Number: K170931 · 2017-11-13

ApplicantCook Incorporated
Decision Date2017-11-13
Product CodeKRA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CXI TriForce Peripheral Crossing Set is the device name listed in this FDA 510(k) record. The listed applicant is Cook Incorporated. It received FDA 510(k) clearance on 2017-11-13 under 510(k) number K170931. The device is classified under product code KRA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CXI TriForce Peripheral Crossing Set?

CXI TriForce Peripheral Crossing Set is a medical device that received FDA 510(k) clearance on 2017-11-13. The listed applicant is Cook Incorporated. The 510(k) number is K170931.

When did CXI TriForce Peripheral Crossing Set receive FDA 510(k) clearance?

CXI TriForce Peripheral Crossing Set received FDA 510(k) clearance on 2017-11-13, under 510(k) number K170931.

Who is the listed applicant for CXI TriForce Peripheral Crossing Set?

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

What is the FDA product code for CXI TriForce Peripheral Crossing Set?

The FDA product code for CXI TriForce Peripheral Crossing Set is KRA.

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Related Devices (Code: KRA)

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.

K261610Verge™ MicrocatheterInstylla, Inc.K260771TruSelect™ 2.6 MicrocatheterBoston Scientific CorporationK250794InVera Infusion DeviceInvera MedicalK243534Micro CatheterSuzhou Zenith Vascular SciTech LimitedK231821XO Cath Microcatheter (E20-090-S, E20-110-S, E20-130-S, E20-150-S, E20-175-S, E20-220-S, E20-090-B, E20-110-B, E20-130-B, E20-150-B, E20-175-B, E20-220-B, E26-090-S, E26-110-S, E26-130-S, E26-150-S, E26-175-S, E26-220-S, E26-090-B, E26-110-B, E26-130-B, E26-150-B, E26-175-B, E26-220-B,)Transit Scientific, LLCK231279Peregrine System Infusion Catheter 4-7 mm, Peregrine System Infusion Catheter 3-4 mmAblative Solutions, Inc.

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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