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FDA 510(k)

BEE Cervical Cage

K-Number: K231371 · 2024-01-12

Decision Date2024-01-12
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BEE Cervical Cage is the device name listed in this FDA 510(k) record. The listed applicant is NGMedical GmbH. It received FDA 510(k) clearance on 2024-01-12 under 510(k) 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. The listed applicant is NGMedical GmbH. The 510(k) number is K231371.

When did BEE Cervical Cage receive FDA 510(k) clearance?

BEE Cervical Cage received FDA 510(k) clearance on 2024-01-12, under 510(k) number K231371.

Who is the listed applicant for BEE Cervical Cage?

The FDA 510(k) record lists NGMedical GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BEE Cervical Cage?

The FDA product code for BEE Cervical Cage is ODP.

Other records listing NGMedical GmbH as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 7 devices →

Related Devices (Code: ODP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.