IMPULSE IQ ADJUSTING INSTRUMENT— 510(k) K080261

Name: FDA 510(k) clearance K080261
Creator: U.S. Food and Drug Administration
Published: 2008-04-11

Substantially Equivalent

Neuromechanical Innovations, LLC

FDA 510(k) clearance K080261 for IMPULSE IQ ADJUSTING INSTRUMENT, Substantially Equivalent on 2008-04-11. Applicant: Neuromechanical Innovations, LLC. Device class: Unclassified.

Clearance details

Applicant: Neuromechanical Innovations, LLC
Product code: Code LXM
Device class: Unclassified
Advisory panel: Unknown
Date received: 2008-02-01
Decision date: 2008-04-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Phoenix, AZ, US

Download summary PDF View on FDA.gov ↗

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