ARTHREX CANNULATED INTERFERENCE SCREW, TITANIUM - FDA Registration MDR-09366A

Access comprehensive regulatory information for ARTHREX CANNULATED INTERFERENCE SCREW, TITANIUM in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09366A and manufactured by Arthrex, Inc. - 1370 Creekside Blvd, Naples Florida 34108-1945,USA in USA. The device was registered on October 28, 2021.

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