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K Number
K001941

Validate with FDA (Live)

Device Name
SYNTHES MODULAR FOOT SYSTEM
Manufacturer
SYNTHES (USA)
Date Cleared
2000-09-22

(88 days)

Product Code
HRS
Regulation Number
888.3030
Type
Traditional
Panel
Orthopedic
Age Range
N/A
Reference & Predicate Devices
N/A
Predicate For
K012655,K021626,K033639,K040907,K050681,K052152,K060474,K060476,K091493,K103705,K113364,K133536,K133541,K142836,K160553,K190750,K190992
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview

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N/A