Multi-unit Abutment Plus

Abutment, Implant, Dental, Endosseous

NOBEL BIOCARE AB

The following data is part of a premarket notification filed by Nobel Biocare Ab with the FDA for Multi-unit Abutment Plus.

Pre-market Notification Details

Device IDK161416
510k NumberK161416
Device Name:Multi-unit Abutment Plus
ClassificationAbutment, Implant, Dental, Endosseous
Applicant NOBEL BIOCARE AB BOX 5190, SE-402 26, VASTRA HAMNAGATAN 1 Goteborg,  SE Se-411 17
ContactCharlemagne Chua
CorrespondentCharlemagne Chua
NOBEL BIOCARE USA LLC 22715 SAVI RANCH PARKWAY Yorba Linda,  CA  92887
Product CodeNHA  
CFR Regulation Number872.3630 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2016-05-23
Decision Date2017-03-16
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
07332747116342 K161416 000
07332747116052 K161416 000
07332747116045 K161416 000
07332747116038 K161416 000
07332747116021 K161416 000
07332747116014 K161416 000
07332747116007 K161416 000
07332747115994 K161416 000
07332747115987 K161416 000
07332747116069 K161416 000
07332747116076 K161416 000
07332747116083 K161416 000
07332747116168 K161416 000
07332747116151 K161416 000
07332747116144 K161416 000
07332747116137 K161416 000
07332747116120 K161416 000
07332747116113 K161416 000
07332747116106 K161416 000
07332747116090 K161416 000
07332747115970 K161416 000

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