ZIMMER PERSONA THE PERSONALIZED KNEE SYSTEM

Prosthesis, Knee, Patello/femorotibial, Semi-constrained, Uncemented, Porous, Coated, Polymer/metal/polymer

ZIMMER, INC.

The following data is part of a premarket notification filed by Zimmer, Inc. with the FDA for Zimmer Persona The Personalized Knee System.

Pre-market Notification Details

Device IDK122745
510k NumberK122745
Device Name:ZIMMER PERSONA THE PERSONALIZED KNEE SYSTEM
ClassificationProsthesis, Knee, Patello/femorotibial, Semi-constrained, Uncemented, Porous, Coated, Polymer/metal/polymer
Applicant ZIMMER, INC. P.O. BOX 708 Warsaw,  IN  46581 -0708
ContactPauline A Shand
CorrespondentPauline A Shand
ZIMMER, INC. P.O. BOX 708 Warsaw,  IN  46581 -0708
Product CodeMBH  
Subsequent Product CodeJWH
Subsequent Product CodeOIY
CFR Regulation Number888.3565 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2012-09-07
Decision Date2012-12-05
Summary:summary

NIH GUDID Devices

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