FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

M-Vizion Femoral Revision System Extension

K Number: K201471 · Decision Jan 11, 2021
Classifications
1
FEI Numbers
284
Registration Numbers
284
Same Product Code
522
Applicant Total
87
Review Days
222

Basic Information

Device Name
M-Vizion Femoral Revision System Extension
K Number
K201471
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3353
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medacta International SA
Date Received
June 3, 2020
Decision Date
January 11, 2021
Product Code
LZO
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
LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

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