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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Attachment, Precision, All
510(k) Number K901928
Device Name INTERPORE IMZ(CASTABLE)TUB/SCRET RET RIGID ATTACH
Applicant
Interpore Intl.
Aba Bioresearch
1700 Rockville Pike, Suite 320
Rockville,  MD  20852
Applicant Contact JOEL S FADEN
Correspondent
Interpore Intl.
Aba Bioresearch
1700 Rockville Pike, Suite 320
Rockville,  MD  20852
Correspondent Contact JOEL S FADEN
Regulation Number872.3165
Classification Product Code
EGG  
Date Received04/27/1990
Decision Date 07/26/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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