IMPLANT CAST TOTAL KNEE REPLACEMENT ARTHROPLASTY, ACS® FB TIBIAL SPACER LATERAL - FDA Registration MDR-09140U

Access comprehensive regulatory information for IMPLANT CAST TOTAL KNEE REPLACEMENT ARTHROPLASTY, ACS® FB TIBIAL SPACER LATERAL in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09140U and manufactured by Implantcast GmbH in Germany. The device was registered on January 15, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (Ilix Medical Implant Trading, 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.