FDA 510(k), K151424, The Progressive Orthopaedic Total Hip System

FDA 510(k), K151424, The Progressive Orthopaedic Total Hip System

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510(K) Number: K151424
Device Name: The Progressive Orthopaedic Total Hip System
Manufacturer: The Progressive Orthopaedic Company, LLC
Device Classification Name: prosthesis, hip, semi-constrained, metal/polymer, porous uncemented
Regulation Number: 888.3358
Classification Product Code: LPH
Date Received: 05/28/2015
Decision Date: 07/27/2016
Regulation Medical Specialty: Orthopedic

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