SYNFIX -LR

Spinal Vertebral Body Replacement Device

SYNTHES SPINE CO.LP

The following data is part of a premarket notification filed by Synthes Spine Co.lp with the FDA for Synfix -lr.

Pre-market Notification Details

Device IDK062083
510k NumberK062083
Device Name:SYNFIX -LR
ClassificationSpinal Vertebral Body Replacement Device
Applicant SYNTHES SPINE CO.LP 1302 WRIGHTS LANE EAST West Chester,  PA  19380
ContactBonnie J Smith
CorrespondentBonnie J Smith
SYNTHES SPINE CO.LP 1302 WRIGHTS LANE EAST West Chester,  PA  19380
Product CodeMQP  
CFR Regulation Number888.3060 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2006-07-21
Decision Date2007-04-03
Summary:summary

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