BONDING BASE

Implant, Endosseous, Root-form

STRAUMANN USA

The following data is part of a premarket notification filed by Straumann Usa with the FDA for Bonding Base.

Pre-market Notification Details

Device IDK973353
510k NumberK973353
Device Name:BONDING BASE
ClassificationImplant, Endosseous, Root-form
Applicant STRAUMANN USA RESERVOIR PLACE, 1601 TRAPELO ROAD Waltham,  MA  02154
ContactLinda Jalbert
CorrespondentLinda Jalbert
STRAUMANN USA RESERVOIR PLACE, 1601 TRAPELO ROAD Waltham,  MA  02154
Product CodeDZE  
CFR Regulation Number872.3640 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1997-09-05
Decision Date1997-12-02
Summary:summary

Trademark Results [BONDING BASE]

Mark Image

Registration | Serial
Company
Trademark
Application Date
BONDING BASE
BONDING BASE
74603401 not registered Dead/Abandoned
MERCER GROUP LTD, THE
1994-11-28

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.