SYNTHES VA LCP ANKLE TRAUMA SYSTEM

Plate, Fixation, Bone

SYNTHES USA

The following data is part of a premarket notification filed by Synthes Usa with the FDA for Synthes Va Lcp Ankle Trauma System.

Pre-market Notification Details

Device IDK120854
510k NumberK120854
Device Name:SYNTHES VA LCP ANKLE TRAUMA SYSTEM
ClassificationPlate, Fixation, Bone
Applicant SYNTHES USA 1301 GOSHEN PKWY West Chester,  PA  19380
ContactAngela F Lassandro
CorrespondentAngela F Lassandro
SYNTHES USA 1301 GOSHEN PKWY West Chester,  PA  19380
Product CodeHRS  
CFR Regulation Number888.3030 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2012-03-21
Decision Date2012-06-18
Summary:summary

NIH GUDID Devices

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