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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Manipulator, Plunger-Like Joint
510(k) Number K072519
Device Name ACTIVATOR V SPINAL ADJUSTING INSTRUMENT
Applicant
Activator Methods International, Ltd.
2751 E. Hale St.
Mesa,  AZ  85313
Applicant Contact DEBBIE KOENEMAN
Correspondent
Activator Methods International, Ltd.
2751 E. Hale St.
Mesa,  AZ  85313
Correspondent Contact DEBBIE KOENEMAN
Classification Product Code
LXM  
Date Received09/07/2007
Decision Date 10/23/2007
Decision Substantially Equivalent (SESE)
510k Review Panel Physical Medicine
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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