FDA 510(k), K031804, COMPRESS DISTAL FEMORAL REPLACEMENT

FDA 510(k), K031804, COMPRESS DISTAL FEMORAL REPLACEMENT

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510(K) Number: K031804
Device Name: COMPRESS DISTAL FEMORAL REPLACEMENT
Manufacturer: BIOMET, INC.
Device Classification Name: prosthesis, knee, femorotibial, constrained, cemented, metal/polymer
Regulation Number: 888.3510
Classification Product Code: KRO
Date Received: 06/11/2003
Decision Date: 12/18/2003
Regulation Medical Specialty: Orthopedic
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