STACKABLE CAGE SYSTEM

Spinal Vertebral Body Replacement Device

DEPUY ACROMED

The following data is part of a premarket notification filed by Depuy Acromed with the FDA for Stackable Cage System.

Pre-market Notification Details

Device IDK001340
510k NumberK001340
Device Name:STACKABLE CAGE SYSTEM
ClassificationSpinal Vertebral Body Replacement Device
Applicant DEPUY ACROMED 325 PARAMOUNT DR. Raynham,  MA  02767 -0350
ContactKaren Jurczak
CorrespondentKaren Jurczak
DEPUY ACROMED 325 PARAMOUNT DR. Raynham,  MA  02767 -0350
Product CodeMQP  
CFR Regulation Number888.3060 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2000-04-27
Decision Date2000-07-26

NIH GUDID Devices

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