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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 K912059
Device Name PRE-ANGLED ABUTMENTS
Applicant
Core-Vent Corp.
1170 Avenida Acaso
Camarillo,  CA  93012
Applicant Contact GLEN NEALLY
Correspondent
Core-Vent Corp.
1170 Avenida Acaso
Camarillo,  CA  93012
Correspondent Contact GLEN NEALLY
Regulation Number872.3640
Classification Product Code
DZE  
Date Received05/09/1991
Decision Date 02/11/1992
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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