ARTHREX FASTHREAD PEEK ROUND DELTA TAPERED INTERFERENCE SCREW WITH DISPOSABLE SHEATH - FDA Registration MDR-10178B

Access comprehensive regulatory information for ARTHREX FASTHREAD PEEK ROUND DELTA TAPERED INTERFERENCE SCREW WITH DISPOSABLE SHEATH in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10178B and manufactured by Arthrex, Inc. in USA. The device was registered on August 06, 2020.

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.