FDA 510(k)

Rebar Micro Catheter

K-Number: K210114 · 2021-02-16

ApplicantMicro Therapeuatics, Inc. D/B/A Ev3 Neurovascular

Decision Date2021-02-16

Product CodeKRA

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

Rebar Micro Catheter is a medical device manufactured by Micro Therapeuatics, Inc. D/B/A Ev3 Neurovascular. It received FDA 510(k) clearance on 2021-02-16 under approval number K210114. 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 Rebar Micro Catheter?

Rebar Micro Catheter is a medical device that received FDA 510(k) clearance on 2021-02-16. It is manufactured by Micro Therapeuatics, Inc. D/B/A Ev3 Neurovascular. The 510(k) number is K210114.

When was Rebar Micro Catheter approved by the FDA?

Rebar Micro Catheter received FDA 510(k) clearance on 2021-02-16, under approval number K210114.

What company makes Rebar Micro Catheter?

Rebar Micro Catheter is manufactured by Micro Therapeuatics, Inc. D/B/A Ev3 Neurovascular.

What is the FDA product code for Rebar Micro Catheter?

The FDA product code for Rebar Micro Catheter is KRA.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.