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FDA 510(k), K173417, Zimmer Persona Personalized Knee System
FDA 510(k), K173417, Zimmer Persona Personalized Knee System
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510(K) Number: K173417
Device Name: Zimmer Persona Personalized Knee System
Manufacturer: Zimmer, Inc.
Device Classification Name: prosthesis, knee, patello/femorotibial, semi-constrained, uncemented, porous, coated, polymer/metal/polymer
Regulation Number: 888.3565
Classification Product Code: MBH
Date Received: 11/01/2017
Decision Date: 01/30/2018
Regulation Medical Specialty: Orthopedic
Device Name: Zimmer Persona Personalized Knee System
Manufacturer: Zimmer, Inc.
Device Classification Name: prosthesis, knee, patello/femorotibial, semi-constrained, uncemented, porous, coated, polymer/metal/polymer
Regulation Number: 888.3565
Classification Product Code: MBH
Date Received: 11/01/2017
Decision Date: 01/30/2018
Regulation Medical Specialty: Orthopedic
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