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U.S. Department of Health and Human Services

Premarket Approval (PMA)

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Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
Classification Nameimplant, endosseous, root-form
Generic Nameimplant, endosseous, root-form
Regulation Number872.3640
lindigstrasse 4
kleinostheim D-638-6380
PMA NumberP800035
Supplement NumberS004
Date Received12/20/1982
Decision Date06/07/1983
Product Code
DZE[ Registered Establishments with DZE ]
Advisory Committee Dental
Expedited Review Granted? No
Combination Product No