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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 the device name listed in this FDA 510(k) record. The listed applicant is Spinalight, Inc.. It received FDA 510(k) clearance on 2018-06-20 under 510(k) 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. The listed applicant is Spinalight, Inc.. The 510(k) number is K172536.

When did Atlas Percussion Adjusting Instrument receive FDA 510(k) clearance?

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

Who is the listed applicant for Atlas Percussion Adjusting Instrument?

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

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

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

Related Devices (Code: LXM)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K234036SONIK MONARK 100Neuro Spinal Innovation, Inc.K192629SpinalyticsOptima Health Solutions International Corp.K160278VSTAAR AdjusteRSpinal Acoustics, LLC

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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