FDA 510(k), K150522, G7 Dual Mobility System

FDA 510(k), K150522, G7 Dual Mobility System

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510(K) Number: K150522
Device Name: G7 Dual Mobility System
Manufacturer: Amy Walriven
Device Classification Name: Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Regulation Number: LPH
Classification Product Code: KXA
Date Received: 03/02/2015
Decision Date: 05/01/2015
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic

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