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510(k) Data Aggregation
K Number
K003649Device Name
TRITON HIP SYSTEMManufacturer
Date Cleared
2001-02-23
(88 days)
Regulation Number
888.3360Type
TraditionalPanel
OrthopedicReference & Predicate Devices
N/A
Why did this record match?
Device Name :
TRITON HIP SYSTEM
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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