gudid Primary ID: 76-CR-0700

Navigated Instrument System (UDI 76-CR-0700)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Navigated Instrument System (Model/Catalog Number: 76-CR-0700) is a medical device manufactured by PRECISION SPINE, INC.. This product is indexed under FDA Product Code / Category Classification NKG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 76-CR-0700
Product Code / EMDN: NKG
Device Name: S-COMP Reform POCT Polyaxial Driver
Database Sync Date: 2026-08-09 09:33:11

Full Regulatory Attributes

🔒 Token Gated

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

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Navigated Instrument System?

The registered manufacturer of record for Navigated Instrument System is PRECISION SPINE, INC..

What is the Primary UDI-DI identifier for Navigated Instrument System?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 76-CR-0700.

What classification code is assigned to this device?

This device is registered under product classification code NKG.

Similar Classification Devices (NKG)

Other Devices by PRECISION SPINE, INC.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint