FDA 510(k), K152494, Zimmer NexGen Complete Knee Solution Tibial and Femoral Augments

510(K) Number: K152494
Device Name: Zimmer NexGen Complete Knee Solution Tibial and Femoral Augments
Manufacturer: ZIMMER, INC.
Device Classification Name: Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Regulation Number: 888.3560
Classification Product Code: JWH
Date Received: 09/01/2015
Decision Date: 11/25/2015
Regulation Medical Specialty: Orthopedic

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