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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 K885159
Device Name MENSOR MAGNASKIRT
Applicant
Merrill C. Mensor, Jr., D.D.S.
P.O. Box 10031
Truckee,  CA  95737
Correspondent
Merrill C. Mensor, Jr., D.D.S.
P.O. Box 10031
Truckee,  CA  95737
Regulation Number872.3640
Classification Product Code
DZE  
Date Received12/13/1988
Decision Date 04/19/1990
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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