ACTIVATOR V SPINAL ADJUSTING INSTRUMENT— 510(k) K072519

Name: FDA 510(k) clearance K072519
Creator: U.S. Food and Drug Administration
Published: 2007-10-23

Substantially Equivalent

Activator Methods International, Ltd.

FDA 510(k) clearance K072519 for ACTIVATOR V SPINAL ADJUSTING INSTRUMENT, Substantially Equivalent on 2007-10-23. Applicant: Activator Methods International, Ltd.. Device class: Unclassified.

Clearance details

Applicant: Activator Methods International, Ltd.
Product code: Code LXM
Device class: Unclassified
Advisory panel: Unknown
Date received: 2007-09-07
Decision date: 2007-10-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mesa, AZ, US

Download summary PDF View on FDA.gov ↗

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