ANKYLOS DENTAL IMPLANT SYSTEM

Implant, Endosseous, Root-form

FRIADENT GMBH

The following data is part of a premarket notification filed by Friadent Gmbh with the FDA for Ankylos Dental Implant System.

Pre-market Notification Details

Device IDK041509
510k NumberK041509
Device Name:ANKYLOS DENTAL IMPLANT SYSTEM
ClassificationImplant, Endosseous, Root-form
Applicant FRIADENT GMBH 21911 ERIE LN. Lake Forest,  CA  92630
ContactCarol Patterson
CorrespondentCarol Patterson
FRIADENT GMBH 21911 ERIE LN. Lake Forest,  CA  92630
Product CodeDZE  
CFR Regulation Number872.3640 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2004-06-07
Decision Date2004-08-26
Summary:summary

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