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VERTEX SELECT® RECONSTRUCTION SYSTEM PLATES - OCCIPITAL MIDLINE PLATE - FDA Registration MDR-08217D

Access comprehensive regulatory information for VERTEX SELECT® RECONSTRUCTION SYSTEM PLATES - OCCIPITAL MIDLINE PLATE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-08217D and manufactured by Medtronic International Limited (Singapore Branch) - Singapore mfd. By: Medtronic Sofamor Danek Manufacturing - Warsaw, IN, USA For: Medtronic Sofamor Danek USA, Inc. - Memphis, TN, USA in USA. The device was registered on July 14, 2021.

This page provides complete registration details including manufacturer information, importer/distributor details (Medtronic Philippines, Inc), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.

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MDR-08217D
VERTEX SELECT® RECONSTRUCTION SYSTEM PLATES - OCCIPITAL MIDLINE PLATE
Registered medical device in Philippines
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Device Information
Product Name
VERTEX SELECT® RECONSTRUCTION SYSTEM PLATES - OCCIPITAL MIDLINE PLATE
Registration Number
MDR-08217D
Importer & Distribution
Importer/Distributor
Medtronic Philippines, Inc
Registration Dates
Issuance Date
July 14, 2021
Expiry Date
May 31, 2025