IXOS Radius Plate System

Plate, Fixation, Bone

Stuckenbrock Medizintechnik GmbH

The following data is part of a premarket notification filed by Stuckenbrock Medizintechnik Gmbh with the FDA for Ixos Radius Plate System.

Pre-market Notification Details

Device IDK171624
510k NumberK171624
Device Name:IXOS Radius Plate System
ClassificationPlate, Fixation, Bone
Applicant Stuckenbrock Medizintechnik GmbH Lessingstraße 50 Tuttlingen,  DE 78532
ContactFabian Stuckenbrock
CorrespondentFabian Stuckenbrock
Stuckenbrock Medizintechnik GmbH Lessingstraße 50 Tuttlingen,  DE 78532
Product CodeHRS  
CFR Regulation Number888.3030 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2017-06-02
Decision Date2018-03-29
Summary:summary

NIH GUDID Devices

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