FDA 510(k), K131684, BIOLOX(R) DELTA CERAMIC HEADS

FDA 510(k), K131684, BIOLOX(R) DELTA CERAMIC HEADS

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510(K) Number: K131684
Device Name: BIOLOX(R) 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: 06/10/2013
Decision Date: 10/10/2013
Regulation Medical Specialty: Orthopedic
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