Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

BEE PLIF Cage

K-Number: K261067 · 2026-04-30

ApplicantNGMedical GmbH
Decision Date2026-04-30
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BEE PLIF Cage is a medical device manufactured by NGMedical GmbH. It received FDA 510(k) clearance on 2026-04-30 under approval number K261067. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEE PLIF Cage?

BEE PLIF Cage is a medical device that received FDA 510(k) clearance on 2026-04-30. It is manufactured by NGMedical GmbH. The 510(k) number is K261067.

When was BEE PLIF Cage approved by the FDA?

BEE PLIF Cage received FDA 510(k) clearance on 2026-04-30, under approval number K261067.

What company makes BEE PLIF Cage?

BEE PLIF Cage is manufactured by NGMedical GmbH.

What is the FDA product code for BEE PLIF Cage?

The FDA product code for BEE PLIF Cage is MAX.

Related Devices (Code: MAX)

K260506Ventana® P/T Lumbar Interbody SystemSpinal Elements, Inc. K260837VersaLift Expandable SystemLife Spine, Inc. K260385aprevo® anterior and lateral lumbar interbody system; aprevo® posterior and transforaminal lumbar interbody system; aprevo® cervical interbody system; corra™ cervical plating systemCarlsmed, Inc.

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.

↑