FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Zimmer Persona Personalized Knee System

K Number: K150090 · Decision May 20, 2015
Classifications
1
FEI Numbers
219
Registration Numbers
219
Same Product Code
133
Applicant Total
308
Review Days
124

Basic Information

Device Name
Zimmer Persona Personalized Knee System
K Number
K150090
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3565
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ZIMMER, INC.
Date Received
January 16, 2015
Decision Date
May 20, 2015
Product Code
MBH
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer

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