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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Attachment, Precision, All
510(k) Number K990979
Device Name STECO-TITANMAGNETICS
Applicant
Steco-System-Technik GmbH & Cokg
Pleicherwall 2
Wurzburg, Bavaria,  DE 97070
Applicant Contact JORN PROBST
Correspondent
Steco-System-Technik GmbH & Cokg
Pleicherwall 2
Wurzburg, Bavaria,  DE 97070
Correspondent Contact JORN PROBST
Regulation Number872.3165
Classification Product Code
EGG  
Date Received03/23/1999
Decision Date 09/03/1999
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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