NuVasive Helix ACP System, Self-Drilling Fixed Screw - FDA Registration MDR-10889G

Access comprehensive regulatory information for NuVasive Helix ACP System, Self-Drilling Fixed Screw in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10889G and manufactured by Nuvasive, Inc. - 7475 Lusk Blvd., San Diego, California, 92121 USA in USA. The device was registered on June 16, 2022.

This page provides complete registration details including manufacturer information, importer/distributor details (Pacificsurgical, 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.