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FDA 510(k)

BEE HA Cage

K-Number: K203444 · 2021-03-18

ApplicantNGMedical GmbH
Decision Date2021-03-18
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BEE HA Cage is a medical device manufactured by NGMedical GmbH. It received FDA 510(k) clearance on 2021-03-18 under approval number K203444. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEE HA Cage?

BEE HA Cage is a medical device that received FDA 510(k) clearance on 2021-03-18. It is manufactured by NGMedical GmbH. The 510(k) number is K203444.

When was BEE HA Cage approved by the FDA?

BEE HA Cage received FDA 510(k) clearance on 2021-03-18, under approval number K203444.

What company makes BEE HA Cage?

BEE HA Cage is manufactured by NGMedical GmbH.

What is the FDA product code for BEE HA Cage?

The FDA product code for BEE HA Cage is ODP.

Other Devices by NGMedical GmbH

K212050NGM WAVE PLIF Cage K211413BEE PLIF Cage K200429BEE Cages K231371BEE Cervical Cage K250560BEE HA K261067BEE PLIF Cage

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K161127The Small PLATEAU (PLATEAU-C) Spacer SystemLife Spine, Inc. K162003IMSE Cervical CageThe Institute of Musculoskeletal Science & Education K160222OIC Cervical PEEK SpacerThe Orthopaedic Implant Company K161809ShurFit CpTi-HA ACIF Interbody Fusion SystemPrecision Spine, Inc. K162220DIO Medical IVA (ACIF, DLIF, PLIF, TLIF,and ALIF) CageDio Medical Co., Ltd. K161649Virtu C Spinal Implant SystemMet 1 Technologies, LLC

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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