KINETIC-SL ANTERIOR CERVICAL PLATE SYSTEM

Appliance, Fixation, Spinal Intervertebral Body

LIFE SPINE

The following data is part of a premarket notification filed by Life Spine with the FDA for Kinetic-sl Anterior Cervical Plate System.

Pre-market Notification Details

Device IDK073479
510k NumberK073479
Device Name:KINETIC-SL ANTERIOR CERVICAL PLATE SYSTEM
ClassificationAppliance, Fixation, Spinal Intervertebral Body
Applicant LIFE SPINE 2401 W. HASSELL RD. SUITE 1535 Hoffman Estates,  IL  60169
ContactRebecca M Brooks
CorrespondentRebecca M Brooks
LIFE SPINE 2401 W. HASSELL RD. SUITE 1535 Hoffman Estates,  IL  60169
Product CodeKWQ  
CFR Regulation Number888.3060 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2007-12-11
Decision Date2008-01-09
Summary:summary

NIH GUDID Devices

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