SYNTHES (USA) LCP DYNAMIC HELICAL HIP SYSTEM

Appliance, Fixation, Nail/blade/plate Combination, Multiple Component

SYNTHES (USA)

The following data is part of a premarket notification filed by Synthes (usa) with the FDA for Synthes (usa) Lcp Dynamic Helical Hip System.

Pre-market Notification Details

Device IDK033556
510k NumberK033556
Device Name:SYNTHES (USA) LCP DYNAMIC HELICAL HIP SYSTEM
ClassificationAppliance, Fixation, Nail/blade/plate Combination, Multiple Component
Applicant SYNTHES (USA) 1690 RUSSELL RD. Paoli,  PA  19301
ContactBonnie Smith
CorrespondentBonnie Smith
SYNTHES (USA) 1690 RUSSELL RD. Paoli,  PA  19301
Product CodeKTT  
CFR Regulation Number888.3030 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2003-11-12
Decision Date2004-01-13
Summary:summary

NIH GUDID Devices

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