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Zimmer Holdings Inc Receives FDA Clearance For Patient Specific Instruments Shoulder


Friday, 23 Aug 2013 10:44am EDT 

Zimmer Holdings, Inc. (NYSE: ZMH; SIX: ZMH), a world leader in musculoskeletal care, today announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market the ZimmerPatient Specific Instruments (PSI) Shoulder system to complement its Trabecular Metal Reverse Shoulder system for reverse shoulder arthroplasty (RSA) procedures. Zimmer PSI Shoulder utilizes 3D visualization software to allow a surgeon to create a customized surgical plan for each patient, and then provides patient-specific surgical instrument guides to facilitate placement of the implant corresponding to the personalized surgical plan. Zimmer PSI Shoulder has been available to a limited number of surgeons in Europe since May and it will now be made available to shoulder surgeons across the United States. 

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103.97
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