BEE Cages

Intervertebral Fusion Device With Bone Graft, Cervical

NGMedical GmbH

The following data is part of a premarket notification filed by Ngmedical Gmbh with the FDA for Bee Cages.

Pre-market Notification Details

Device IDK200429
510k NumberK200429
Device Name:BEE Cages
ClassificationIntervertebral Fusion Device With Bone Graft, Cervical
Applicant NGMedical GmbH Talsperrenblick 5 Nonnweiler,  DE 66620
ContactStella Hahn
CorrespondentChristine Scifert
MRC Global 9085 East Mineral Circle, Suite 110 Centennial,  CO  80112
Product CodeODP  
CFR Regulation Number888.3080 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2020-02-21
Decision Date2021-01-29

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