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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Mixer, Cement, For Clinical Use
510(k) Number K760617
Device Name MIX EVAC BONE CEMENT
Applicant
Stryker Corp.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Stryker Corp.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number888.4210
Classification Product Code
JDZ  
Date Received09/13/1976
Decision Date 10/05/1976
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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