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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 K870331
Device Name IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTS
Applicant
Interpore Intl.
18008 Skypark Cir.
Irvine,  CA  92714
Applicant Contact JO STEGWELL
Correspondent
Interpore Intl.
18008 Skypark Cir.
Irvine,  CA  92714
Correspondent Contact JO STEGWELL
Regulation Number872.3165
Classification Product Code
EGG  
Date Received01/28/1987
Decision Date 03/02/1987
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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