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FDA 510(k)

NEXTSTEP RETROGRADE

K-Number: K130192 · 2013-05-10

ApplicantArrow International, Inc.
Decision Date2013-05-10
Product CodeMSD
Advisory CommitteeGU
DecisionUnknown

Device Summary

NEXTSTEP RETROGRADE is the device name listed in this FDA 510(k) record. The listed applicant is Arrow International, Inc.. It received FDA 510(k) clearance on 2013-05-10 under 510(k) number K130192. The device is classified under product code MSD. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the NEXTSTEP RETROGRADE?

NEXTSTEP RETROGRADE is a medical device that received FDA 510(k) clearance on 2013-05-10. The listed applicant is Arrow International, Inc.. The 510(k) number is K130192.

When did NEXTSTEP RETROGRADE receive FDA 510(k) clearance?

NEXTSTEP RETROGRADE received FDA 510(k) clearance on 2013-05-10, under 510(k) number K130192.

Who is the listed applicant for NEXTSTEP RETROGRADE?

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

What is the FDA product code for NEXTSTEP RETROGRADE?

The FDA product code for NEXTSTEP RETROGRADE is MSD.

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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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