ORTHOLOC 3DI ANKLE FUSION PLATING SYSTEM

Plate, Fixation, Bone

WRIGHT MEDICAL TECHNOLOGY, INC.

The following data is part of a premarket notification filed by Wright Medical Technology, Inc. with the FDA for Ortholoc 3di Ankle Fusion Plating System.

Pre-market Notification Details

Device IDK121425
510k NumberK121425
Device Name:ORTHOLOC 3DI ANKLE FUSION PLATING SYSTEM
ClassificationPlate, Fixation, Bone
Applicant WRIGHT MEDICAL TECHNOLOGY, INC. 5677 AIRLINE RD. Arlington,  TN  38002
ContactSamir Ibrahim
CorrespondentSamir Ibrahim
WRIGHT MEDICAL TECHNOLOGY, INC. 5677 AIRLINE RD. Arlington,  TN  38002
Product CodeHRS  
CFR Regulation Number888.3030 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2012-05-14
Decision Date2012-10-01
Summary:summary

NIH GUDID Devices

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