STRAUMANN NARROW NECK IMPLANTS

Implant, Endosseous, Root-form

STRAUMANN USA

The following data is part of a premarket notification filed by Straumann Usa with the FDA for Straumann Narrow Neck Implants.

Pre-market Notification Details

Device IDK060958
510k NumberK060958
Device Name:STRAUMANN NARROW NECK IMPLANTS
ClassificationImplant, Endosseous, Root-form
Applicant STRAUMANN USA 60 MINUTEMAN ROAD Andover,  MA  01810
ContactElaine Alan
CorrespondentElaine Alan
STRAUMANN USA 60 MINUTEMAN ROAD Andover,  MA  01810
Product CodeDZE  
CFR Regulation Number872.3640 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2006-04-07
Decision Date2006-08-24
Summary:summary

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