SoSuperior™ Knee System - Femoral Component Medial Pivot (Left) - FDA Registration CMDR-2024-02412A

Access comprehensive regulatory information for SoSuperior™ Knee System - Femoral Component Medial Pivot (Left) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-02412A and manufactured by Suzhou MicroPort OrthoRecon Co., Ltd. 316, Bldg. 2, No.112, Fangzhong Street, Suzhou Industrial Park, 215000, Suzhou Jiangsu, People's Republic of China in China. The device was registered on March 05, 2024.

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.