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Found 1 results

510(k) Data Aggregation

K Number

Validate with FDA (Live)

Device Name

SYNTHES MODULAR FOOT SYSTEM

Manufacturer

Date Cleared

2000-09-22

(88 days)

Product Code

Regulation Number

Type

Panel

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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