Arthrex® Mini Tightrope® FT with Corkscrew - FDA Registration MDR-10049K

Access comprehensive regulatory information for Arthrex® Mini Tightrope® FT with Corkscrew in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10049K and manufactured by Arthrex, Inc. - 1370 Creekside Boulevard, Naples, Florida 34108-1945, USA in USA. The device was registered on August 22, 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.