FRIOS MICROSAW

Handpiece, Rotary Bone Cutting

FRIADENT GMBH

The following data is part of a premarket notification filed by Friadent Gmbh with the FDA for Frios Microsaw.

Pre-market Notification Details

Device IDK994298
510k NumberK994298
Device Name:FRIOS MICROSAW
ClassificationHandpiece, Rotary Bone Cutting
Applicant FRIADENT GMBH 21911 ERIE LN. Lake Forest,  CA  92630
ContactCarol Patterson
CorrespondentCarol Patterson
FRIADENT GMBH 21911 ERIE LN. Lake Forest,  CA  92630
Product CodeKMW  
CFR Regulation Number872.4120 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1999-12-21
Decision Date2000-02-18
Summary:summary

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