MODULAR REPLACEMENT SYSTEM CEMENTED STEMS

Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/polymer

HOWMEDICA OSTEONICS CORP

The following data is part of a premarket notification filed by Howmedica Osteonics Corp with the FDA for Modular Replacement System Cemented Stems.

Pre-market Notification Details

Device IDK040749
510k NumberK040749
Device Name:MODULAR REPLACEMENT SYSTEM CEMENTED STEMS
ClassificationProsthesis, Knee, Femorotibial, Constrained, Cemented, Metal/polymer
Applicant HOWMEDICA OSTEONICS CORP 325 CORPORATE DR. Mahwah,  NJ  07430
ContactMargaret F Crowe
CorrespondentMargaret F Crowe
HOWMEDICA OSTEONICS CORP 325 CORPORATE DR. Mahwah,  NJ  07430
Product CodeKRO  
CFR Regulation Number888.3510 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2004-03-23
Decision Date2004-06-17
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
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