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510(k) Data Aggregation
K Number
K091000Device Name
KNEEKG
Manufacturer
EMOVI
Date Cleared
2009-10-26
(201 days)
Product Code
LXJ
Regulation Number
890.5360Why did this record match?
Applicant Name (Manufacturer) :
EMOVI
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
Measure and analyze 3D position and movement by placing markers on the knees of patients whose movement function is to be assessed.
Device Description
The KneeKG measures and analyzes the 3D position and movement of electromagnetic markers placed on the knee of patients whose movement function is to be assessed. The movement data are acquired into a host PC which then analyses and displays the data on graphs and printed reports.
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