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

MyPAO Planning Report

K Number: K200589 · Decision Feb 19, 2021
Classifications
1
FEI Numbers
599
Registration Numbers
599
Same Product Code
2271
Applicant Total
165
Review Days
350

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Basic Information

Device Name
MyPAO Planning Report
K Number
K200589
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medacta International S.A.
Date Received
March 6, 2020
Decision Date
February 19, 2021
Product Code
LLZ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
LLZ System, Image Processing, Radiological

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