FDA.reportPublic FDA data

510(k) K072519

Device
ACTIVATOR V SPINAL ADJUSTING INSTRUMENT
Applicant
Activator Methods International, Ltd.
510(k) number
K072519
Product code
LXM
Decision
Substantially Equivalent (SESE)
Decision date
2007-10-23
Date received
2007-09-07
Classification name
Manipulator, Plunger-Like Joint
Medical specialty
Unknown
Review panel
Unknown
Device class
U
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
DEBBIE KOENEMAN
Address
2751 E. Hale St. Mesa AZ US 85313 85313

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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K021238FRYE ADJUSTING INSTRUMENTFrye Health Systems2002-10-09
K010851HARRISON HAND HELD ADJUSTING INSTRUMENTHarrison Cbp Seminars2001-09-18
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K001476TORQUE INSTRUMENT, MODEL 8500Spinalight, Inc.2000-08-04