gudid Primary ID: LP01-1703

Elatus Lumbar Plate System (UDI LP01-1703)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Elatus Lumbar Plate System (Model/Catalog Number: LP01-1703) is a medical device manufactured by Aegis Spine, Inc.. This product is indexed under FDA Product Code / Category Classification LXH within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: LP01-1703
Product Code / EMDN: LXH
Device Name: Plate Holder
Database Sync Date: 2026-08-09 09:12:08

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 Elatus Lumbar Plate System?

The registered manufacturer of record for Elatus Lumbar Plate System is Aegis Spine, Inc..

What is the Primary UDI-DI identifier for Elatus Lumbar Plate System?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is LP01-1703.

What classification code is assigned to this device?

This device is registered under product classification code LXH.

Similar Classification Devices (LXH)

Other Devices by Aegis Spine, Inc.

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