FDA 510(k), K060515, DEPUY PFC SIGMA KNEE PROSTHESIS
FDA 510(k), K060515, DEPUY PFC SIGMA KNEE PROSTHESIS
Device Name: DEPUY PFC SIGMA KNEE PROSTHESIS
Manufacturer:
Device Classification Name: Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Regulation Number: 888.3560
Classification Product Code: JWH
Date Received: 02/27/2006
Decision Date: 03/23/2006
Regulation Medical Specialty: Orthopedic
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