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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Methyl Methacrylate For Cranioplasty
510(k) Number K040152
Device Name BONE CEMENT FOR CRANIOPLASTY
Applicant
Cardinalhealth
1500 Waukegan Rd.
Bldg. Wm
Mcgaw Park,  IL  60085
Applicant Contact SHARON NICHOLS
Correspondent
Cardinalhealth
1500 Waukegan Rd.
Bldg. Wm
Mcgaw Park,  IL  60085
Correspondent Contact SHARON NICHOLS
Regulation Number882.5300
Classification Product Code
GXP  
Date Received01/23/2004
Decision Date 05/19/2004
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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