Atlas Percussion Adjusting Instrument— 510(k) K172536

Name: FDA 510(k) clearance K172536
Creator: U.S. Food and Drug Administration
Published: 2018-06-20

Substantially Equivalent

Spinalight, Inc.

FDA 510(k) clearance K172536 for Atlas Percussion Adjusting Instrument, Substantially Equivalent on 2018-06-20. Applicant: Spinalight, Inc.. Device class: Unclassified.

Clearance details

Applicant: Spinalight, Inc.
Product code: Code LXM
Device class: Unclassified
Advisory panel: Unknown
Date received: 2017-08-22
Decision date: 2018-06-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Petersburg, FL, US

Download summary PDF View on FDA.gov ↗

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