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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Implant, Endosseous, Root-Form
510(k) Number K963121
Device Name FIXTURE MOUNT KIT
Applicant
Steri-Oss, Inc.
22895 Eastpark Dr.
Yorba Linda,  CA  92887
Applicant Contact PAUL GASSER
Correspondent
Steri-Oss, Inc.
22895 Eastpark Dr.
Yorba Linda,  CA  92887
Correspondent Contact PAUL GASSER
Regulation Number872.3640
Classification Product Code
DZE  
Date Received08/12/1996
Decision Date 11/05/1996
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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