Fx Shoulder USA, Inc.
Fx Shoulder USA, Inc. holds FDA 510(k) medical device clearances, first cleared 2019, most recent 2024.
Top product codes for Fx Shoulder USA, Inc.
Recent clearances by Fx Shoulder USA, Inc.
- K240278 — Full Wedge Lateralized and Augmented Baseplates
- K223801 — FX V135(TM) Shoulder Prosthesis
- K222936 — Humeris® 135 Shoulder System
- K213117 — FX V135 Shoulder Prosthesis
- K210790 — Lateralized and Augmented Baseplates
- K201391 — Easytech® Anatomical Shoulder System
- K191698 — TiN Coated Humeral Head
- K191146 — Humelock TiN Coated Glenosphere
- K193394 — Humeral Cup Stability & Humeral Cup 135/145o Stability
- K192799 — Glenoid Baseplate with Screw
- K192206 — 32mm Glenosphere and Humeral Cup
Data sourced from openFDA. This site is unofficial and independent of the FDA.