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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 K885158
Device Name MENSOR COMPLIANT KEEPER
Applicant
Merrill C. Mensor, Jr., D.D.S.
P.O. Box 10031
Truckee,  CA  95737
Applicant Contact MERRILL C MENSOR
Correspondent
Merrill C. Mensor, Jr., D.D.S.
P.O. Box 10031
Truckee,  CA  95737
Correspondent Contact MERRILL C MENSOR
Regulation Number872.3640
Classification Product Code
DZE  
Date Received12/13/1988
Decision Date 06/06/1991
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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