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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 K960110
Device Name KIS MT3
Applicant
The Implant Center of the Palm Beaches
824 Us Hwy. 1
Suite 370
N. Palm Beach,  FL  33408
Applicant Contact JACK T KRAUSER
Correspondent
The Implant Center of the Palm Beaches
824 Us Hwy. 1
Suite 370
N. Palm Beach,  FL  33408
Correspondent Contact JACK T KRAUSER
Regulation Number872.3640
Classification Product Code
DZE  
Date Received01/11/1996
Decision Date 03/20/1996
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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