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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 K873939
Device Name ADI/B/*/HA-2 STAGE OSSEO. HYDRO. DENTAL IMPLANT
Applicant
Anchor Implants , Ltd.
1190 W. 8th Ave.
Vancouver, B.C.
Canada,  CA V6H 3Z4
Applicant Contact DR. H BERGMAN
Correspondent
Anchor Implants , Ltd.
1190 W. 8th Ave.
Vancouver, B.C.
Canada,  CA V6H 3Z4
Correspondent Contact DR. H BERGMAN
Regulation Number872.3640
Classification Product Code
DZE  
Date Received09/28/1987
Decision Date 03/15/1988
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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