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FDA 510(k)

AltiVate Anatomic to Reverse Conversion Module

K-Number: K173073 · 2017-12-26

ApplicantEncore Medical L.P.
Decision Date2017-12-26
Product CodePHX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AltiVate Anatomic to Reverse Conversion Module is a medical device manufactured by Encore Medical L.P.. It received FDA 510(k) clearance on 2017-12-26 under approval number K173073. 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 AltiVate Anatomic to Reverse Conversion Module?

AltiVate Anatomic to Reverse Conversion Module is a medical device that received FDA 510(k) clearance on 2017-12-26. It is manufactured by Encore Medical L.P.. The 510(k) number is K173073.

When was AltiVate Anatomic to Reverse Conversion Module approved by the FDA?

AltiVate Anatomic to Reverse Conversion Module received FDA 510(k) clearance on 2017-12-26, under approval number K173073.

What company makes AltiVate Anatomic to Reverse Conversion Module?

AltiVate Anatomic to Reverse Conversion Module is manufactured by Encore Medical L.P..

What is the FDA product code for AltiVate Anatomic to Reverse Conversion Module?

The FDA product code for AltiVate Anatomic to Reverse Conversion Module is PHX.

Related PubMed Literature

PMID: 39857002 TransRAUNet: A Deep Neural Network with Reverse Attention Module Using HU Windowing Augmentation for Robust Liver Vessel Segmentation in Full Resolution of CT Images. Diagnostics (Basel, Switzerland) (2025)

Other Devices by Encore Medical L.P.

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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. K170414Arthrex Univers Revers Apex Humeral StemsArthrex, Inc. K171058Medacta Shoulder System: Threaded Glenoid BaseplateMedacta International S.A.

Official Source

View on FDA Database →

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

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