eudamed_udi Primary ID: 10888857455894

CASCADIA™ Interbody System (UDI 10888857455894)

Manufactured by K2M, Inc.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The CASCADIA™ Interbody System (Model/Catalog Number: 6101-90866) is a medical device manufactured by K2M, Inc.. This product is indexed under FDA Product Code / Category Classification L0915 within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 1 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-1307-2022 View Full Alert →

Yukon Straight Rod 4.0 x120mm; Cat# 7601-540120. Used to provide immobilization and stabilization of spinal segments....

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Technical Specifications

Model Number: 6101-90866
Product Code / EMDN: L0915
Device Name: Cascadia: Spreader
Database Sync Date: 2026-08-09 16:29:36

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of CASCADIA™ Interbody System?

The registered manufacturer of record for CASCADIA™ Interbody System is K2M, Inc..

What is the Primary UDI-DI identifier for CASCADIA™ Interbody System?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10888857455894.

What classification code is assigned to this device?

This device is registered under product classification code L0915.

Similar Classification Devices (L0915)

Other Devices by K2M, Inc.

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