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510(k) Data Aggregation
K Number
K953439Device Name
ULTRACK TOTAL KNEE SYSTEMManufacturer
Date Cleared
1996-01-30
(193 days)
Product Code
Regulation Number
888.3560Type
TraditionalPanel
Orthopedic (OR)Reference & Predicate Devices
N/A
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Device Name :
ULTRACK TOTAL KNEE SYSTEM
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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