FDA 510(k), K051411, ARCOMXL POLYETHYLENE LINERS AND BIOLOX DELTA HEADS

FDA 510(k), K051411, ARCOMXL POLYETHYLENE LINERS AND BIOLOX DELTA HEADS

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510(K) Number: K051411
Device Name: ARCOMXL POLYETHYLENE LINERS AND BIOLOX DELTA HEADS
Manufacturer:
Device Classification Name: Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
Regulation Number: 888.3353
Classification Product Code: LZO
Date Received: 05/31/2005
Decision Date: 06/29/2005
Regulation Medical Specialty: Orthopedic
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