NuVasive VuePoint II OCT System - Set Screw, Tulip and Laminar Hook
Philippines·NuVasive, Inc. 7475 Lusk blvd. San Diego, California 92121, USA·USA·Issued March 20, 2024 – March 20, 2029- Product Name
- NuVasive VuePoint II OCT System - Set Screw, Tulip and Laminar Hook
- Registration Number
- CMDR-2024-02451B
- Country of Origin
- USA
- Importer/Distributor
- PacificSurgical Inc.
- Issuance Date
- March 20, 2024
- Expiry Date
- March 20, 2029
Access comprehensive regulatory information for NuVasive VuePoint II OCT System - Set Screw, Tulip and Laminar Hook in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-02451B 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.