FDA Product Code: 00-5990-014-02 00-5990-015-02 00-5992-016-02

Name: FDA Product Code 00-5990-014-02 00-5990-015-02 00-5992-016-02 Device Index
Creator: GUDIDData Intelligence
License: https://creativecommons.org/publicdomain/zero/1.0/

Directory of devices assigned to product classification code 00-5990-014-02 00-5990-015-02 00-5992-016-02.

enforcement LPS PRECOAT FEM SIZE D-RT LPS PRECOAT FEM SIZE E-RT LPS POROUS FEM SIZE F-RT This device is indicated for patients with severe knee pain and disability Manufacturer: Zimmer Biomet, Inc.

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