FDA 510(k)

ARROW Reverse Porous Glenoid

K-Number: K171789 · 2018-01-23

ApplicantFournitures Hospitalieres Industrie

Decision Date2018-01-23

Product CodePHX

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

ARROW Reverse Porous Glenoid is a medical device manufactured by Fournitures Hospitalieres Industrie. It received FDA 510(k) clearance on 2018-01-23 under approval number K171789. The device is classified under product code PHX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARROW Reverse Porous Glenoid?

ARROW Reverse Porous Glenoid is a medical device that received FDA 510(k) clearance on 2018-01-23. It is manufactured by Fournitures Hospitalieres Industrie. The 510(k) number is K171789.

When was ARROW Reverse Porous Glenoid approved by the FDA?

ARROW Reverse Porous Glenoid received FDA 510(k) clearance on 2018-01-23, under approval number K171789.

What company makes ARROW Reverse Porous Glenoid?

ARROW Reverse Porous Glenoid is manufactured by Fournitures Hospitalieres Industrie.

What is the FDA product code for ARROW Reverse Porous Glenoid?

The FDA product code for ARROW Reverse Porous Glenoid is PHX.

Other Devices by Fournitures Hospitalieres Industrie

K163148BePOD® Foot Screws K163710BePOD® EZ Weil Screws K162068ARROW Anatomical Porous glenoid K170040BePOD Cannulated Arthrodesis Screws

Related Devices (Code: PHX)

K161742Aequalis PerFORM Reversed, Aequalis PerFORM+ Reversed GlenoidTornier, Inc. K161189Integra TITAN Reverse Shoulder SystemIntegra LifeSciences Corporation K152754COMPREHENSIVE VAULT RECONSTRUCTION SYSTEM (VRS)Biomet Manufacturing Corp K152966Aequalis Fx2Tornier S.A.S. K173073AltiVate Anatomic to Reverse Conversion ModuleEncore Medical L.P. K170414Arthrex Univers Revers Apex Humeral StemsArthrex, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.