MICROFIX QUICKANCHOR PLUS

Screw, Fixation, Bone

MITEK WORLDWIDE

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

Pre-market Notification Details

Device IDK024115
510k NumberK024115
Device Name:MICROFIX QUICKANCHOR PLUS
ClassificationScrew, Fixation, Bone
Applicant MITEK WORLDWIDE 249 VANDERBILT AVE. Norwood,  MA  02062
ContactRuth C Forstadt
CorrespondentRuth C Forstadt
MITEK WORLDWIDE 249 VANDERBILT AVE. Norwood,  MA  02062
Product CodeHWC  
CFR Regulation Number888.3040 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2002-12-13
Decision Date2003-03-13
Summary:summary

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