ARTHREX CANNULATED INTERFERENCE SCREW, TITANIUM
Philippines·Arthrex, Inc. - 1370 Creekside Blvd, Naples Florida 34108-1945,USA·USA·Issued October 28, 2021 – March 25, 2026- Product Name
- ARTHREX CANNULATED INTERFERENCE SCREW, TITANIUM
- Registration Number
- MDR-09366A
- Country of Origin
- USA
- Importer/Distributor
- Pacific Surgical, Inc.
- Issuance Date
- October 28, 2021
- Expiry Date
- March 25, 2026
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.