TITANIUM MINIPLATE SYSTEM

Plate, Bone

MEDICON, E.G.

The following data is part of a premarket notification filed by Medicon, E.g. with the FDA for Titanium Miniplate System.

Pre-market Notification Details

Device IDK951690
510k NumberK951690
Device Name:TITANIUM MINIPLATE SYSTEM
ClassificationPlate, Bone
Applicant MEDICON, E.G. 24301 ROBERTS DR. SUITE C Black Diamond,  WA  98010
ContactDennis Youde
CorrespondentDennis Youde
MEDICON, E.G. 24301 ROBERTS DR. SUITE C Black Diamond,  WA  98010
Product CodeJEY  
CFR Regulation Number872.4760 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1995-04-05
Decision Date1995-07-26

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