SUPER QUICKANCHOR PLUS

Staple, Fixation, Bone

Depuy Mitek

The following data is part of a premarket notification filed by Depuy Mitek with the FDA for Super Quickanchor Plus.

Pre-market Notification Details

Device IDK041116
510k NumberK041116
Device Name:SUPER QUICKANCHOR PLUS
ClassificationStaple, Fixation, Bone
Applicant Depuy Mitek 249 VANDERBILT AVE. Norwood,  MA  02062
ContactAllyson Barford
CorrespondentAllyson Barford
Depuy Mitek 249 VANDERBILT AVE. Norwood,  MA  02062
Product CodeJDR  
CFR Regulation Number888.3030 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2004-04-29
Decision Date2004-05-28
Summary:summary

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