FDA 510(k), K030941, AEQUALIS REVERSED SHOULDER PROSTHESIS

FDA 510(k), K030941, AEQUALIS REVERSED SHOULDER PROSTHESIS

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510(K) Number: K030941
Device Name: AEQUALIS REVERSED SHOULDER PROSTHESIS
Manufacturer: TORNIER
Device Classification Name: shoulder prosthesis, reverse configuration
Regulation Number: 888.3660
Classification Product Code: PHX
Date Received: 03/25/2003
Decision Date: 05/14/2004
Regulation Medical Specialty: Orthopedic

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