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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name bone grafting material, synthetic
510(k) Number K840260
Device Name PERIOGRAF DURAPATITE 40-60 MESH
Applicant
STERLING DRUG, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
STERLING DRUG, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number872.3930
Classification Product Code
LYC  
Date Received01/10/1984
Decision Date 04/05/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
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