gudid Primary ID: 59-SP-0720

Reform MC Screw System (UDI 59-SP-0720)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Reform MC Screw System (Model/Catalog Number: 59-SP-0720) is a medical device manufactured by PRECISION SPINE, INC.. This product is indexed under FDA Product Code / Category Classification HXX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 59-SP-0720
Product Code / EMDN: HXX
Device Name: Modular Screw Driver
Database Sync Date: 2026-08-09 09:33:11

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 Reform MC Screw System?

The registered manufacturer of record for Reform MC Screw System is PRECISION SPINE, INC..

What is the Primary UDI-DI identifier for Reform MC Screw System?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 59-SP-0720.

What classification code is assigned to this device?

This device is registered under product classification code HXX.

Similar Classification Devices (HXX)

Other Devices by PRECISION SPINE, INC.

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