NuVasive VuePoint II OCT System -Screw, Tulip and Keel Plate - FDA Registration CMDR-2024-02451S

Access comprehensive regulatory information for NuVasive VuePoint II OCT System -Screw, Tulip and Keel Plate in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-02451S and manufactured by NuVasive, Inc. 7475 Lusk blvd. San Diego, California 92121, USA in USA. The device was registered on March 20, 2024.

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.