FDA 510(k), K110542, CONSENSUS BIOLOX DELTA CERAMIC FEMORAL HEAD

FDA 510(k), K110542, CONSENSUS BIOLOX DELTA CERAMIC FEMORAL HEAD

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510(K) Number: K110542
Device Name: CONSENSUS BIOLOX DELTA CERAMIC FEMORAL HEAD
Manufacturer:
Device Classification Name: Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Regulation Number: 888.3358
Classification Product Code: LPH
Date Received: 02/24/2011
Decision Date: 04/01/2011
Regulation Medical Specialty: Orthopedic
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