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FDA 510(k)

SPIN-SWI

K-Number: K173224 · 2018-02-23

ApplicantSpintech, Inc.
Decision Date2018-02-23
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SPIN-SWI is a medical device manufactured by Spintech, Inc.. It received FDA 510(k) clearance on 2018-02-23 under approval number K173224. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPIN-SWI?

SPIN-SWI is a medical device that received FDA 510(k) clearance on 2018-02-23. It is manufactured by Spintech, Inc.. The 510(k) number is K173224.

When was SPIN-SWI approved by the FDA?

SPIN-SWI received FDA 510(k) clearance on 2018-02-23, under approval number K173224.

What company makes SPIN-SWI?

SPIN-SWI is manufactured by Spintech, Inc..

What is the FDA product code for SPIN-SWI?

The FDA product code for SPIN-SWI is LNH.

Other Devices by Spintech, Inc.

K210843STAGE K223079Stage

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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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