FDA 510(k), K042091, BIOLOX DELTA CERAMIC HEADS

FDA 510(k), K042091, BIOLOX DELTA CERAMIC HEADS

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510(K) Number: K042091
Device Name: BIOLOX DELTA CERAMIC 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: 08/03/2004
Decision Date: 03/25/2005
Regulation Medical Specialty: Orthopedic
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