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FDA 510(k)

Atlas Percussion Adjusting Instrument

K-Number: K172536 · 2018-06-20

ApplicantSpinalight, Inc.
Decision Date2018-06-20
Product CodeLXM
DecisionSubstantially Equivalent

Device Summary

Atlas Percussion Adjusting Instrument is a medical device manufactured by Spinalight, Inc.. It received FDA 510(k) clearance on 2018-06-20 under approval number K172536. The device is classified under product code LXM. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Atlas Percussion Adjusting Instrument?

Atlas Percussion Adjusting Instrument is a medical device that received FDA 510(k) clearance on 2018-06-20. It is manufactured by Spinalight, Inc.. The 510(k) number is K172536.

When was Atlas Percussion Adjusting Instrument approved by the FDA?

Atlas Percussion Adjusting Instrument received FDA 510(k) clearance on 2018-06-20, under approval number K172536.

What company makes Atlas Percussion Adjusting Instrument?

Atlas Percussion Adjusting Instrument is manufactured by Spinalight, Inc..

What is the FDA product code for Atlas Percussion Adjusting Instrument?

The FDA product code for Atlas Percussion Adjusting Instrument is LXM.

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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.

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