FDA 510(k), K083762, BIOLOX DELTA CERAMIC FEMORAL HEADS

FDA 510(k), K083762, BIOLOX DELTA CERAMIC FEMORAL HEADS

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510(K) Number: K083762
Device Name: BIOLOX DELTA CERAMIC FEMORAL 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: 12/18/2008
Decision Date: 03/11/2009
Regulation Medical Specialty: Orthopedic
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