BEE HA Cage

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 Ha Cage.

Pre-market Notification Details

Device IDK203444
510k NumberK203444
Device Name:BEE HA Cage
ClassificationIntervertebral Fusion Device With Bone Graft, Cervical
Applicant NGMedical GmbH Talsperrenblick 5 Nonnweiler,  DE 66620
ContactStella Hahn
CorrespondentChristine Scifert
MRC Global, LLC 9085 E. Mineral Cir., Suite 110 Centennial,  CO  80112
Product CodeODP  
CFR Regulation Number888.3080 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2020-11-23
Decision Date2021-03-18

© 2021 FDA.report
This site is not affiliated with or endorsed by the FDA.