FDA 510(k), K103120, CORIN BIOLOX DELTA FEMORAL HEADS
FDA 510(k), K103120, CORIN BIOLOX DELTA FEMORAL HEADS
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510(K) Number: K103120
Device Name: CORIN BIOLOX DELTA 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: 10/22/2010
Decision Date: 02/28/2011
Regulation Medical Specialty: Orthopedic
Device Name: CORIN BIOLOX DELTA 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: 10/22/2010
Decision Date: 02/28/2011
Regulation Medical Specialty: Orthopedic