BePOD Cannulated Arthrodesis Screws

Screw, Fixation, Bone

Fournitures Hospitalieres Industrie

The following data is part of a premarket notification filed by Fournitures Hospitalieres Industrie with the FDA for Bepod Cannulated Arthrodesis Screws.

Pre-market Notification Details

Device IDK170040
510k NumberK170040
Device Name:BePOD Cannulated Arthrodesis Screws
ClassificationScrew, Fixation, Bone
Applicant Fournitures Hospitalieres Industrie ZI De Kernevez - 6 Rue Nobel Quimper,  FR 29000
ContactPatricia Donnard
CorrespondentPatricia Donnard
Fournitures Hospitalieres Industrie ZI De Kernevez - 6 Rue Nobel Quimper,  FR 29000
Product CodeHWC  
CFR Regulation Number888.3040 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2017-01-05
Decision Date2017-04-04

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
03661489562143 K170040 000
03661489684319 K170040 000
03661489684326 K170040 000
03661489684333 K170040 000
03661489684340 K170040 000
03661489684357 K170040 000
03661489684364 K170040 000
03661489384585 K170040 000
03661489451065 K170040 000
03661489475788 K170040 000
03661489537134 K170040 000
03661489537141 K170040 000
03661489537158 K170040 000
03661489537165 K170040 000
03661489537172 K170040 000
03661489537189 K170040 000
03661489537196 K170040 000
03661489537882 K170040 000
03661489684302 K170040 000

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