BEE Cervical Cage
K-Number: K231371 · 2024-01-12
ApplicantNGMedical GmbH
Decision Date2024-01-12
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
BEE Cervical Cage is a medical device manufactured by NGMedical GmbH. It received FDA 510(k) clearance on 2024-01-12 under approval number K231371. 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 Cervical Cage?
BEE Cervical Cage is a medical device that received FDA 510(k) clearance on 2024-01-12. It is manufactured by NGMedical GmbH. The 510(k) number is K231371.
When was BEE Cervical Cage approved by the FDA?
BEE Cervical Cage received FDA 510(k) clearance on 2024-01-12, under approval number K231371.
What company makes BEE Cervical Cage?
BEE Cervical Cage is manufactured by NGMedical GmbH.
What is the FDA product code for BEE Cervical Cage?
The FDA product code for BEE Cervical Cage is ODP.
Other Devices by NGMedical GmbH
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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.