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510(k) Data Aggregation
K Number
K011083Manufacturer
Date Cleared
2001-06-28
(79 days)
Product Code
Regulation Number
888.1100Type
TraditionalPanel
OrthopedicReference & Predicate Devices
N/A
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Device Name :
ARTHROCARE SYSTEM 2000 CONTROLLER, CABLE, FOOTSWITCH, POWER CORD & ARTHROCARE ARTHROWAND
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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