Stryker SternalPlate System

Plate, Fixation, Bone

Stryker

The following data is part of a premarket notification filed by Stryker with the FDA for Stryker Sternalplate System.

Pre-market Notification Details

Device IDK183172
510k NumberK183172
Device Name:Stryker SternalPlate System
ClassificationPlate, Fixation, Bone
Applicant Stryker 750 Trade Centre Way, Suite 200 Portage,  MI  49002
ContactHans Geiger
CorrespondentHans Geiger
Stryker 750 Trade Centre Way, Suite 200 Portage,  MI  49002
Product CodeHRS  
CFR Regulation Number888.3030 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2018-11-16
Decision Date2019-03-05

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
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