Palti Bone (UDI G520MD48150)

Manufactured by Medspo

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Palti Bone (Model/Catalog Number: MD4815) is a medical device manufactured by Medspo. This product is indexed under FDA Product Code / Category Classification Q010302 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: MD4815
Product Code / EMDN: Q010302
Device Name: Palti Bone
Database Sync Date: 2026-08-09 16:49:06

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 Palti Bone?

The registered manufacturer of record for Palti Bone is Medspo.

What is the Primary UDI-DI identifier for Palti Bone?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G520MD48150.

What classification code is assigned to this device?

This device is registered under product classification code Q010302.

Similar Classification Devices (Q010302)

Other Devices by Medspo

Programmatic Export

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

JSON API Endpoint