ANTEROLATERAL AND MEDIAL LOCKING PLATING SYSTEM

Plate, Fixation, Bone

DEPUY ORTHOPAEDICS, INC.

The following data is part of a premarket notification filed by Depuy Orthopaedics, Inc. with the FDA for Anterolateral And Medial Locking Plating System.

Pre-market Notification Details

Device IDK072832
510k NumberK072832
Device Name:ANTEROLATERAL AND MEDIAL LOCKING PLATING SYSTEM
ClassificationPlate, Fixation, Bone
Applicant DEPUY ORTHOPAEDICS, INC. 700 ORTHOPAEDIC DRIVE Warsaw,  IN  46581 -0988
ContactSuzana Otano
CorrespondentSuzana Otano
DEPUY ORTHOPAEDICS, INC. 700 ORTHOPAEDIC DRIVE Warsaw,  IN  46581 -0988
Product CodeHRS  
CFR Regulation Number888.3030 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2007-10-03
Decision Date2007-12-14
Summary:summary

NIH GUDID Devices

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