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FDA 510(k) K043547, COMPRESS SEGMENTAL FEMORAL REPLACEMENT SYSTEM, by Biomet, Inc.

FDA 510(k) K043547, COMPRESS SEGMENTAL FEMORAL REPLACEMENT SYSTEM, by Biomet, Inc.

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510(K) Number: K043547
Device Name: COMPRESS SEGMENTAL FEMORAL REPLACEMENT SYSTEM
Manufacturer: Biomet, Inc.
Device Classification Name: prosthesis, hip, semi-constrained (metal uncemented acetabular component)
Regulation Number: 888.3330
Classification Product Code: KWA
Date Received: 12/23/2004
Decision Date: 08/05/2005
Regulation Medical Specialty: Orthopedic
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