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 a medical device manufactured by Cook Incorporated. It received FDA 510(k) clearance on 2017-11-13 under approval 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. It is manufactured by Cook Incorporated. The 510(k) number is K170931.
When was CXI TriForce Peripheral Crossing Set approved by the FDA?
CXI TriForce Peripheral Crossing Set received FDA 510(k) clearance on 2017-11-13, under approval number K170931.
What company makes CXI TriForce Peripheral Crossing Set?
CXI TriForce Peripheral Crossing Set is manufactured by Cook Incorporated.
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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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.