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FDA 510(k) K041352, COMPRESS DISTAL FEMORAL REPLACEMENT SYSTEM, by Biomet, Inc.

FDA 510(k) K041352, COMPRESS DISTAL FEMORAL REPLACEMENT SYSTEM, by Biomet, Inc.

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510(K) Number: K041352
Device Name: COMPRESS DISTAL FEMORAL REPLACEMENT SYSTEM
Manufacturer: Biomet, Inc.
Device Classification Name: prosthesis, knee, femorotibial, constrained, cemented, metal/polymer
Regulation Number: 888.3510
Classification Product Code: KRO
Date Received: 05/20/2004
Decision Date: 07/30/2004
Regulation Medical Specialty: Orthopedic
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