Pyrenees Cervical Plate System

Appliance, Fixation, Spinal Intervertebral Body

K2M

The following data is part of a premarket notification filed by K2m with the FDA for Pyrenees Cervical Plate System.

Pre-market Notification Details

Device IDK153526
510k NumberK153526
Device Name:Pyrenees Cervical Plate System
ClassificationAppliance, Fixation, Spinal Intervertebral Body
Applicant K2M 751 MILLER DRIVE SE Leesburg,  VA  20175
ContactNancy Giezen
CorrespondentNancy Giezen
K2M 751 MILLER DRIVE SE Leesburg,  VA  20175
Product CodeKWQ  
CFR Regulation Number888.3060 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2015-12-09
Decision Date2016-04-27
Summary:summary

NIH GUDID Devices

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